b>j)΄!Pԫ&;"kB޶}pSVT(wę!j x;-m@JnQ+պכ7MajfJͱ4jѲ撆RxZMz7vIW/dٞТזcZM~ji ߒsQzԠDW3Den"M+/B:-uIJ7j委9p='mANޭ=/B:-n&nUfqxZM~c Ϲ+,&ᾺܢF[(1*" ϒ"Jԧ<;b" "jܢF[x ,!q қ*]/؝27SMcs"ޭDQ/应ܢF_! :s" 7`F+SVTn"IJnQ/应B 4 wD"IJ׭-`S9DrjiEJ߅gJ应矁[xZM~n"IB؃!'Тѕ+(mIKʭ/|ϐܢF[xZMzG %嬩/c[[ Antibiotics Archives - Prosel Pharma | Trusted Healthcare Solutions https://proselpharma.com/product-category/antibiotics/ Trusted Healthcare Solutions Thu, 25 Jun 2026 01:12:00 +0000 en-US hourly 1 https://wordpress.org/?v=6.9.4 https://proselpharma.com/wp-content/uploads/2026/03/favicon-100x100.png Antibiotics Archives - Prosel Pharma | Trusted Healthcare Solutions https://proselpharma.com/product-category/antibiotics/ 32 32 SELZEF® Suspension https://proselpharma.com/product/selzef-suspension/ Fri, 06 Mar 2026 07:19:48 +0000 https://prosel.imanilahost.com/?post_type=product&p=1023 Cefalexin is an antibacterial agent of the cephalosporin class. Like other cephalosporin, cefalexin exerts antibacterial activity by binding to and inhibiting the action of penicillin-binding proteins involved in the synthesis of bacterial cell walls. This leads to bacterial cell lysis and cell death. Cefalexin is acid stable and is readily absorbed after oral administration. Food may delay absorption. Intramuscular doses of the lysine salt are well absorbed but up to 15% of a dose is bound to plasma proteins. The half-life had been reported to range from 0.5 to 2 hours and this increases with reduced renal function. Cefalexin is widely distributed in the body but does not enter the cerebrospinal fluid in significant quantities. It diffuses across the placenta and small quantities are found in the milk of nursing mothers. About 80% or more of a dose is excreted unchanged in the urine in the first 6 hours by glomerular filtration and tubular secretion.

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]]> Cefalexin is an antibacterial agent of the cephalosporin class. Like other cephalosporin, cefalexin exerts antibacterial activity by binding to and inhibiting the action of penicillin-binding proteins involved in the synthesis of bacterial cell walls. This leads to bacterial cell lysis and cell death.

Cefalexin is acid stable and is readily absorbed after oral administration. Food may delay absorption. Intramuscular doses of the lysine salt are well absorbed but up to 15% of a dose is bound to plasma proteins. The half-life had been reported to range from 0.5 to 2 hours and this increases with reduced renal function. Cefalexin is widely distributed in the body but does not enter the cerebrospinal fluid in significant quantities. It diffuses across the placenta and small quantities are found in the milk of nursing mothers. About 80% or more of a dose is excreted unchanged in the urine in the first 6 hours by glomerular filtration and tubular secretion.

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]]> Selzef 500mg Capsule https://proselpharma.com/product/selzef-500mg-capsule/ Fri, 06 Mar 2026 06:49:01 +0000 https://prosel.imanilahost.com/?post_type=product&p=1018 Cefalexin is an antibacterial agent of the cephalosporin class. Like other cephalosporin, cefalexin exerts antibacterial activity by binding to and inhibiting the action of penicillin-binding proteins involved in the synthesis of bacterial cell walls. This leads to bacterial cell lysis and cell death. Cefalexin is acid stable and is readily absorbed after oral administration. Food may delay absorption. Intramuscular doses of the lysine salt are well absorbed but up to 15% of a dose is bound to plasma proteins. The half-life had been reported to range from 0.5 to 2 hours and this increases with reduced renal function. Cefalexin is widely distributed in the body but does not enter the cerebrospinal fluid in significant quantities. It diffuses across the placenta and small quantities are found in the milk of nursing mothers. About 80% or more of a dose is excreted unchanged in the urine in the first 6 hours by glomerular filtration and tubular secretion.

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]]> Cefalexin is an antibacterial agent of the cephalosporin class. Like other cephalosporin, cefalexin exerts antibacterial activity by binding to and inhibiting the action of penicillin-binding proteins involved in the synthesis of bacterial cell walls. This leads to bacterial cell lysis and cell death.

Cefalexin is acid stable and is readily absorbed after oral administration. Food may delay absorption. Intramuscular doses of the lysine salt are well absorbed but up to 15% of a dose is bound to plasma proteins. The half-life had been reported to range from 0.5 to 2 hours and this increases with reduced renal function. Cefalexin is widely distributed in the body but does not enter the cerebrospinal fluid in significant quantities. It diffuses across the placenta and small quantities are found in the milk of nursing mothers. About 80% or more of a dose is excreted unchanged in the urine in the first 6 hours by glomerular filtration and tubular secretion.

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]]> Promox 250mg/5mL Suspension https://proselpharma.com/product/promox-250mg-5ml-suspension/ Wed, 04 Mar 2026 03:19:57 +0000 https://prosel.imanilahost.com/?post_type=product&p=908 Off-white to light peach powder which yields orange color upon reconstitution, with orange flavor. Amoxicillin is a semisynthetic penicillin (beta-lactam antibiotic) that inhibits one or more enzymes (often referred to as penicillin- binding proteins, PBPs) in the biosynthetic pathway of bactericidal peptidoglycan, which is an integral structural component of the bacterial cell wall. Inhibition of peptidoglycan synthesis leads to weakening of the cell wall, which is usually followed by cell lysis and death. Amoxicillin is susceptible to degradation by beta-lactamases produced by resistant bacteria and therefore the spectrum of activity of amoxicillin alone does not include organisms which produce these enzymes.

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]]> Off-white to light peach powder which yields orange color upon reconstitution, with orange flavor.

Amoxicillin is a semisynthetic penicillin (beta-lactam antibiotic) that inhibits one or more enzymes (often referred to as penicillin- binding proteins, PBPs) in the biosynthetic pathway of bactericidal peptidoglycan, which is an integral structural component of the bacterial cell wall. Inhibition of peptidoglycan synthesis leads to weakening of the cell wall, which is usually followed by cell lysis and death.

Amoxicillin is susceptible to degradation by beta-lactamases produced by resistant bacteria and therefore the spectrum of activity of amoxicillin alone does not include organisms which produce these enzymes.

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]]> Zindal 300mg Capsule https://proselpharma.com/product/zindal-300mg-capsule/ Tue, 03 Mar 2026 04:05:42 +0000 https://prosel.imanilahost.com/?post_type=product&p=879 Clindamycin is a lincosamide antibiotic, which is chlorinated derivative of lincomycin with a primarily bacteriostatic action against Gram-positive organisms and a wide range of anaerobic pathogens, as well as some antiprotozoal actions. Lincosamides such as clindamycin bind to the 50S subunit of the bacterial ribosome similarly to macrolides such as erythromycin and inhibit the early stages of protein synthesis. It is usually used when other drugs are unsuitable, in the treatment of anaerobic, staphylococcal and streptococcal infections, and in the prophylaxis of endocarditis. It has also been tried in Pneumocystis carinii pneumonia and in protozoal infections such as babesiosis, malaria and toxoplasmosis.

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]]> Clindamycin is a lincosamide antibiotic, which is chlorinated derivative of lincomycin with a primarily bacteriostatic action against Gram-positive organisms and a wide range of anaerobic pathogens, as well as some antiprotozoal actions. Lincosamides such as clindamycin bind to the 50S subunit of the bacterial ribosome similarly to macrolides such as erythromycin and inhibit the early stages of protein synthesis. It is usually used when other drugs are unsuitable, in the treatment of anaerobic, staphylococcal and streptococcal infections, and in the prophylaxis of endocarditis. It has also been tried in Pneumocystis carinii pneumonia and in protozoal infections such as babesiosis, malaria and toxoplasmosis.

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]]> Selzef 100mg/mL Drops https://proselpharma.com/product/selzef-100mg-ml-drops/ Tue, 03 Mar 2026 03:47:34 +0000 https://prosel.imanilahost.com/?post_type=product&p=876 Cefalexin is an antibacterial agent of the cephalosporin class. Like other cephalosporin, cefalexin exerts antibacterial activity by binding to and inhibiting the action of penicillin-binding proteins involved in the synthesis of bacterial cell walls. This leads to bacterial cell lysis and cell death. Cefalexin is acid stable and is readily absorbed after oral administration. Food may delay absorption. Intramuscular doses of the lysine salt are well absorbed but up to 15% of a dose is bound to plasma proteins. The half-life had been reported to range from 0.5 to 2 hours and this increases with reduced renal function. Cefalexin is widely distributed in the body but does not enter the cerebrospinal fluid in significant quantities. It diffuses across the placenta and small quantities are found in the milk of nursing mothers. About 80% or more of a dose is excreted unchanged in the urine in the first 6 hours by glomerular filtration and tubular secretion.

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]]> Cefalexin is an antibacterial agent of the cephalosporin class. Like other cephalosporin, cefalexin exerts antibacterial activity by binding to and inhibiting the action of penicillin-binding proteins involved in the synthesis of bacterial cell walls. This leads to bacterial cell lysis and cell death.

Cefalexin is acid stable and is readily absorbed after oral administration. Food may delay absorption. Intramuscular doses of the lysine salt are well absorbed but up to 15% of a dose is bound to plasma proteins. The half-life had been reported to range from 0.5 to 2 hours and this increases with reduced renal function. Cefalexin is widely distributed in the body but does not enter the cerebrospinal fluid in significant quantities. It diffuses across the placenta and small quantities are found in the milk of nursing mothers. About 80% or more of a dose is excreted unchanged in the urine in the first 6 hours by glomerular filtration and tubular secretion.

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]]> PROMOX 500 mg Capsule https://proselpharma.com/product/promox-500-mg-capsule/ Fri, 27 Feb 2026 08:09:50 +0000 https://prosel.imanilahost.com/?post_type=product&p=872 White or almost white, crystalline or semi-granular powder encapsulated in capsule size #0 with orange cap and light gray body.   Amoxicillin is a semisynthetic penicillin (beta-lactam antibiotic) that inhibits one or more enzymes (often referred to as penicillin- binding proteins, PBPs) in the biosynthetic pathway of bactericidal peptidoglycan, which is an integral structural component of the bacterial cell wall. Inhibition of peptidoglycan synthesis leads to weakening of the cell wall, which is usually followed by cell lysis and death.   Amoxicillin is susceptible to degradation by beta-lactamases produced by resistant bacteria and therefore the spectrum of activity of amoxicillin alone does not include organisms which produce these enzymes.

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]]> White or almost white, crystalline or semi-granular powder encapsulated in capsule size #0 with orange cap and light gray body.  

Amoxicillin is a semisynthetic penicillin (beta-lactam antibiotic) that inhibits one or more enzymes (often referred to as penicillin- binding proteins, PBPs) in the biosynthetic pathway of bactericidal peptidoglycan, which is an integral structural component of the bacterial cell wall. Inhibition of peptidoglycan synthesis leads to weakening of the cell wall, which is usually followed by cell lysis and death.  

Amoxicillin is susceptible to degradation by beta-lactamases produced by resistant bacteria and therefore the spectrum of activity of amoxicillin alone does not include organisms which produce these enzymes.

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]]> Procor 200mg/40mg Suspension https://proselpharma.com/product/procor-200mg-40mg-suspension/ Fri, 27 Feb 2026 08:03:05 +0000 https://prosel.imanilahost.com/?post_type=product&p=869 Light orange suspension with orange/butterscoth flavor.  After oral administration trimethoprim and sulfamethoxazole are rapidly and nearly completely absorbed. The presence of food does not appear to delay absorption. Peak levels in the blood occur between one and four hours after ingestion and the level attained is dose related. Effective levels persist in the blood for up to 24 hours after a therapeutic dose. Steady state levels in adults are reached after dosing for 2-3 days. Neither component has an appreciable effect on the concentrations achieved in the blood by the other. Trimethoprim is a weak base with a pKa of 7.4. It is lipophilic. Tissue levels of trimethoprim are generally higher than corresponding plasma levels, the lungs and kidneys showing especially high concentrations. Trimethoprim concentrations exceed those in plasma in the case of bile, prostatic fluid and tissue, saliva, sputum and vaginal secretions. Levels in the aqueous humor, breast milk, cerebrospinal fluid, middle ear fluid, synovial fluid and tissue (intestinal) fluid are adequate for antibacterial activity. Trimethoprim passes into amniotic fluid and foetal tissues reaching concentrations approximating those of maternal serum. About 45% of trimethoprim in the plasma is protein bound. The half-life in man is in the range 8.6 to 17 hours in the presence of normal renal function. It is increased by a factor of 1.5 to 3.0 when the creatinine clearance is less than 10 ml/minute. There appears to be no significant difference in the elderly compared with young patients. The principal route of excretion of trimethoprim is renal and approximately 50% of the dose is excreted in the urine within 24 hours as unchanged drug. Several metabolites have been identified in the urine. Urinary concentrations of trimethoprim vary widely. ulfamethoxazole is a weak acid with a pKa of 6.0. The concentration of active sulfamethoxazole in a variety of body fluids is of the order of 20 to 50% of the plasma concentration. Approximately 66% of sulfamethoxazole in the plasma is protein bound and the principal route of excretion of sulfamethoxazole is renal. The half-life in man is approximately 9 to 11 hours in the presence of normal renal function. There is no change in the half-life of active sulfamethoxazole with a reduction in renal function but there is prolongation of the half-life of the major, acetylated metabolite when the creatinine clearance is below 25 ml/minute. The principle route of excretion of sulfamethoxazole is renal; between 15% and 30% of the dose recovered in the urine is in the active form. In elderly patients there is a reduced renal clearance of sulfamethoxazole.

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]]> Light orange suspension with orange/butterscoth flavor. 

After oral administration trimethoprim and sulfamethoxazole are rapidly and nearly completely absorbed. The presence of food does not appear to delay absorption. Peak levels in the blood occur between one and four hours after ingestion and the level attained is dose related. Effective levels persist in the blood for up to 24 hours after a therapeutic dose. Steady state levels in adults are reached after dosing for 2-3 days. Neither component has an appreciable effect on the concentrations achieved in the blood by the other. Trimethoprim is a weak base with a pKa of 7.4. It is lipophilic. Tissue levels of trimethoprim are generally higher than corresponding plasma levels, the lungs and kidneys showing especially high concentrations. Trimethoprim concentrations exceed those in plasma in the case of bile, prostatic fluid and tissue, saliva, sputum and vaginal secretions. Levels in the aqueous humor, breast milk, cerebrospinal fluid, middle ear fluid, synovial fluid and tissue (intestinal) fluid are adequate for antibacterial activity. Trimethoprim passes into amniotic fluid and foetal tissues reaching concentrations approximating those of maternal serum. About 45% of trimethoprim in the plasma is protein bound. The half-life in man is in the range 8.6 to 17 hours in the presence of normal renal function. It is increased by a factor of 1.5 to 3.0 when the creatinine clearance is less than 10 ml/minute. There appears to be no significant difference in the elderly compared with young patients. The principal route of excretion of trimethoprim is renal and approximately 50% of the dose is excreted in the urine within 24 hours as unchanged drug. Several metabolites have been identified in the urine. Urinary concentrations of trimethoprim vary widely.

ulfamethoxazole is a weak acid with a pKa of 6.0. The concentration of active sulfamethoxazole in a variety of body fluids is of the order of 20 to 50% of the plasma concentration. Approximately 66% of sulfamethoxazole in the plasma is protein bound and the principal route of excretion of sulfamethoxazole is renal. The half-life in man is approximately 9 to 11 hours in the presence of normal renal function. There is no change in the half-life of active sulfamethoxazole with a reduction in renal function but there is prolongation of the half-life of the major, acetylated metabolite when the creatinine clearance is below 25 ml/minute. The principle route of excretion of sulfamethoxazole is renal; between 15% and 30% of the dose recovered in the urine is in the active form. In elderly patients there is a reduced renal clearance of sulfamethoxazole.

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]]> KXD 125mg/5mL Suspension https://proselpharma.com/product/kxd-125mg-5ml-suspension/ Fri, 27 Feb 2026 07:56:47 +0000 https://prosel.imanilahost.com/?post_type=product&p=866 Clarithromycin is a semi-synthetic derivative of erythromycin. It exerts its antibacterial action by binding to the 50s ribosomal sub-unit of susceptible bacteria and suppresses protein synthesis. It is highly potent against a wide variety of aerobic and anaerobic gram-positive and gram-negative organisms.

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]]> Clarithromycin is a semi-synthetic derivative of erythromycin. It exerts its antibacterial action by binding to the 50s ribosomal sub-unit of susceptible bacteria and suppresses protein synthesis. It is highly potent against a wide variety of aerobic and anaerobic gram-positive and gram-negative organisms.

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]]> Inovox 625mg Tablet https://proselpharma.com/product/inovox-625mg-tablet/ Fri, 27 Feb 2026 07:08:50 +0000 https://prosel.imanilahost.com/?post_type=product&p=849 Co-amoxiclav (Inovox) 625 mg is a white to off-white film coated tablet, biconvex, oval shaped and plain on both sides, Co-amoxiclav is an oral antibacterial combination consisting of the synthetic antibiotic amoxicillin and B- lactamase inhibitor, clavulanate potassium (the potassium salt of clavulanic acid). Amoxicillin Trihydrate is an analog of ampicillin, derived from the basic penicillin nucleus, 6-aminopenicillanic acid. The Amoxicillin Trihydrate molecular formula is C16H, 9N3O5S«3H2O, and the molecular weight is 419.46. Chemically, amoxicillin is (2S, 5R, 6R)-6[(R)-(-)-2-Amino-2 (4-hydroxyphenyl) acetamido]-3, 3-dimethyl-7-oxo-4-thia-1-azabicycl o [3.2.0] heptane-2-carboxylic acid trihydrate and may be represented structurally as: Clavulanic acid is produced by fermentation of Streptomyces clavuligerus. It is a B-lactam structurally related to the penicillins and possesses the ability to inactivate a wide variety of B-lactamases by blocking the active sites of these enzymes. Clavulanic acid is particularly active against the clinically important plasmid-mediated B-lactamases frequently responsible for transferred drug resistance to penicillins and cephalosporins. The clavulanate potassium molecular formula is C9HSKNO5, and the molecular weight is 237.25. Chemically, clavulanate potassium is potassium (ZH2R,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]-heptane-2-carboxylat e and may be represented structurally as:

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]]> Co-amoxiclav (Inovox) 625 mg is a white to off-white film coated tablet, biconvex, oval shaped and plain on both sides, Co-amoxiclav is an oral antibacterial combination consisting of the synthetic antibiotic amoxicillin and B- lactamase inhibitor, clavulanate potassium (the potassium salt of clavulanic acid). Amoxicillin Trihydrate is an analog of ampicillin, derived from the basic penicillin nucleus, 6-aminopenicillanic acid. The Amoxicillin Trihydrate molecular formula is C16H, 9N3O5S«3H2O, and the molecular weight is 419.46. Chemically, amoxicillin is (2S, 5R, 6R)-6[(R)-(-)-2-Amino-2 (4-hydroxyphenyl) acetamido]-3, 3-dimethyl-7-oxo-4-thia-1-azabicycl o [3.2.0] heptane-2-carboxylic acid trihydrate and may be represented structurally as:

Clavulanic acid is produced by fermentation of Streptomyces clavuligerus. It is a B-lactam structurally related to the penicillins and possesses the ability to inactivate a wide variety of B-lactamases by blocking the active sites of these enzymes. Clavulanic acid is particularly active against the clinically important plasmid-mediated B-lactamases frequently responsible for transferred drug resistance to penicillins and cephalosporins. The clavulanate potassium molecular formula is C9HSKNO5, and the molecular weight is 237.25. Chemically, clavulanate potassium is potassium (ZH2R,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]-heptane-2-carboxylat e and may be represented structurally as:

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]]> Inovox 400mg/57mg Suspension https://proselpharma.com/product/inovox-400mg-57mg-suspension/ Thu, 26 Feb 2026 04:03:31 +0000 https://prosel.imanilahost.com/?post_type=product&p=766 Co-amoxiclav is an oral antibacterial combination consisting of the synthetic antibiotic amoxicillin and P-lactamase inhibitor, clavulanate potassium (the potassium salt of clavulanic acid). Amoxicillin is an analog of ampicillin, derived from the basic penicillin nucleus, 6-aminopenicillanic acid. The amoxicillin molecular formula is C16H19N3O5S•3H2O, and the molecular weight is 419.46. -Chemically, amoxicillin is (2S, 5R,6R)-6[(R)-(-)-2-Amino-2(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid trihydrate and may be represented structurally as: Clavulanic acid is produced by fermentation of Streptomyces clavuligerus. It is a b-lactam structurally related to the penicillins and possesses the ability to inactivate a wide variety of b-lactamases by blocking the active sites of these enzymes. Clavulanic acid is particularly active against the clinically important plasmid mediated b-lactamases frequently responsible for transferred drug resistance to penicillins and cephalosporins. The clavulanate potassium molecular formula is C8H8KNO5, and the molecular weight is 237.25. Chemically, clavulanate potassium is potassium (Z)-(2R,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo [3.2.0]-heptane-2-carboxylate and may be represented structurally as:

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]]> Co-amoxiclav is an oral antibacterial combination consisting of the synthetic antibiotic amoxicillin and P-lactamase inhibitor, clavulanate potassium (the potassium salt of clavulanic acid). Amoxicillin is an analog of ampicillin, derived from the basic penicillin nucleus, 6-aminopenicillanic acid. The amoxicillin molecular formula is C16H19N3O5S•3H2O, and the molecular weight is 419.46. -Chemically, amoxicillin is (2S, 5R,6R)-6[(R)-(-)-2-Amino-2(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid trihydrate and may be represented structurally as:

Clavulanic acid is produced by fermentation of Streptomyces clavuligerus. It is a b-lactam structurally related to the penicillins and possesses the ability to inactivate a wide variety of b-lactamases by blocking the active sites of these enzymes. Clavulanic acid is particularly active against the clinically important plasmid mediated b-lactamases frequently responsible for transferred drug resistance to penicillins and cephalosporins. The clavulanate potassium molecular formula is C8H8KNO5, and the molecular weight is 237.25. Chemically, clavulanate potassium is potassium (Z)-(2R,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo [3.2.0]-heptane-2-carboxylate and may be represented structurally as:

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]]>