FDA NDC Directory · JSON-LD · Markdown

Acyclovir

NDC 51655-679 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203834
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (800 mg/1)
Marketing started20230215
Package count3

External sources

Source: openFDA. Public-domain (CC0).