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Acyclovir

NDC 69452-291 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209366
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (800 mg/1)
Marketing started20200815
Package count2

External sources

Source: openFDA. Public-domain (CC0).