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Amoxicillin

NDC 76420-573 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA061931
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (250 mg/5mL)
Marketing started19900930
Package count3

External sources

Source: openFDA. Public-domain (CC0).