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Amoxicillin

NDC 0143-9889 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065322
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (250 mg/5mL)
Marketing started20060619
Package count3

External sources

Source: openFDA. Public-domain (CC0).