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Cefaclor

NDC 0093-1087 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065058
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsCEFACLOR (500 mg/1)
Marketing started20020926
Package count1

External sources

Source: openFDA. Public-domain (CC0).