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Acyclovir

NDC 71335-1053 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA075382
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (400 mg/1)
Marketing started20091022
Package count10

External sources

Source: openFDA. Public-domain (CC0).