FDA NDC Directory · JSON-LD · Markdown

acyclovir

NDC 68071-5100 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077309
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (800 mg/1)
Marketing started20060313
Marketing ended20261231
Package count1

External sources

Source: openFDA. Public-domain (CC0).