FDA NDC Directory · JSON-LD · Markdown

Acyclovir

NDC 17856-0083 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA074738
Dosage form / routeSUSPENSION · ORAL
Active ingredientsACYCLOVIR (200 mg/5mL)
Marketing started20020903
Package count2

External sources

Source: openFDA. Public-domain (CC0).