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Amoxicillin

NDC 76420-819 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065378
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (400 mg/5mL)
Marketing started20070326
Package count3

External sources

Source: openFDA. Public-domain (CC0).