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Amoxicillin

NDC 76420-838 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065256
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMOXICILLIN (500 mg/1)
Marketing started20051109
Package count2

External sources

Source: openFDA. Public-domain (CC0).