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Acyclovir

NDC 63187-253 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203834
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (400 mg/1)
Marketing started20131129
Package count6

External sources

Source: openFDA. Public-domain (CC0).