FDA NDC Directory · JSON-LD · Markdown

ACYCLOVIR

NDC 70518-4186 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA074891
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (800 mg/1)
Marketing started20240925
Package count1

External sources

Source: openFDA. Public-domain (CC0).