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Each 250-mg capsule contains cefaclor monohydrate equivalent to 250 mg (0.68 mmol) of anhydrous cefaclor and inactive ingredients: magnesium stearate,sodium starch glycolate, lactose monohydrate, talc.  The 250 mg capsule shell contains gelatin, titanium dioxide, and imprinting ink components: shellac, strong ammonia solution, potassium hydroxide, black iron oxide, dehydrated alcohol, isopropyl alcohol, butyl alcohol and propylene glycol.
Each 250-mg capsule contains cefaclor monohydrate equivalent to 250 mg (0.68 mmol) of anhydrous cefaclor and inactive ingredients: magnesium stearate,sodium starch glycolate, lactose monohydrate, talc.  The 250 mg capsule shell contains gelatin, titanium dioxide, and imprinting ink components: shellac, strong ammonia solution, potassium hydroxide, black iron oxide, dehydrated alcohol, isopropyl alcohol, butyl alcohol and propylene glycol.


Each 500-mg capsule contains cefaclor monohydrate equivalent to 500 mg (1.36 mmol) of anhydrous cefaclor and inactive ingredients: magnesium stearate,sodium starch glycolate, lactose monohydrate, talc. The 500 mg capsule shell contains gelatin, titanium dioxide, and imprinting ink components: shellac, strong ammonia solution, titanium dioxide, aluminum lake, dehydrated alcohol, isopropyl alcohol, butyl alcohol and propylene glycol.
Each 500-mg capsule contains cefaclor monohydrate equivalent to 500 mg (1.36 mmol) of anhydrous cefaclor and inactive ingredients: magnesium stearate,sodium starch glycolate, lactose monohydrate, talc. The 500 mg capsule shell contains gelatin, titanium dioxide, and imprinting ink components: shellac, strong ammonia solution, titanium dioxide, aluminum lake, dehydrated alcohol, isopropyl alcohol, butyl alcohol and propylene glycol.<ref>{{Cite web | last = |first = |title = http://www.accessdata.fda.gov/drugsatfda_docs/nda/98/64081_Cefaclor_Approv.pdf |url =http://www.accessdata.fda.gov/drugsatfda_docs/nda/98/64081_Cefaclor_Approv.pdf publisher = |date = | accessdate = }}</ref>
 
==References==
==References==
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{{Reflist}}

Revision as of 15:26, 24 December 2013

Cefaclor
CECLOR® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Clinical Studies
Dosage and Administration
How Supplied
Labels and Packages

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Description

Cefaclor, USP is a semisynthetic cephalosporin antibiotic for oral administration. It is chemically designated as 3-chloro-7-D-(2-phenylglycinamido) -3-cephem-4-carboxylic acid monohydrate. The chemical formula for cefaclor is C15H14ClN3O4S·H2O and the molecular weight is 385.82.

Each 250-mg capsule contains cefaclor monohydrate equivalent to 250 mg (0.68 mmol) of anhydrous cefaclor and inactive ingredients: magnesium stearate,sodium starch glycolate, lactose monohydrate, talc. The 250 mg capsule shell contains gelatin, titanium dioxide, and imprinting ink components: shellac, strong ammonia solution, potassium hydroxide, black iron oxide, dehydrated alcohol, isopropyl alcohol, butyl alcohol and propylene glycol.

Each 500-mg capsule contains cefaclor monohydrate equivalent to 500 mg (1.36 mmol) of anhydrous cefaclor and inactive ingredients: magnesium stearate,sodium starch glycolate, lactose monohydrate, talc. The 500 mg capsule shell contains gelatin, titanium dioxide, and imprinting ink components: shellac, strong ammonia solution, titanium dioxide, aluminum lake, dehydrated alcohol, isopropyl alcohol, butyl alcohol and propylene glycol.[1]

References

  1. publisher = "http://www.accessdata.fda.gov/drugsatfda_docs/nda/98/64081_Cefaclor_Approv.pdf" Check |url= value (help). External link in |title= (help)

Adapted from the FDA Package Insert.


References

Adapted from the FDA Package Insert.