FDA NDC Directory · JSON-LD · Markdown

ACYCLOVIR

NDC 60687-867 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA074891
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (800 mg/1)
Marketing started20250606
Package count1

External sources

Source: openFDA. Public-domain (CC0).