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Amoxicillin

NDC 68788-8852 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065325
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (200 mg/5mL)
Marketing started20250324
Package count1

External sources

Source: openFDA. Public-domain (CC0).