FDA NDC Directory · JSON-LD · Markdown

Acyclovir

NDC 31722-681 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215669
Dosage form / routeSUSPENSION · ORAL
Active ingredientsACYCLOVIR (200 mg/5mL)
Marketing started20220701
Package count1

External sources

Source: openFDA. Public-domain (CC0).