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Acyclovir

NDC 54348-627 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPharmPak, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203834
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (400 mg/1)
Marketing started20131129
Package count7

External sources

Source: openFDA. Public-domain (CC0).