FDA NDC Directory · JSON-LD · Markdown

acyclovir

NDC 71205-391 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077309
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (400 mg/1)
Marketing started20070609
Package count4

External sources

Source: openFDA. Public-domain (CC0).