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Amoxicillin

NDC 68071-4969 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065387
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (125 mg/5mL)
Marketing started20070326
Package count1

External sources

Source: openFDA. Public-domain (CC0).