FDA NDC Directory · JSON-LD · Markdown

ACYCLOVIR

NDC 23155-229 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameacyclovir
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074889
Dosage form / routeCAPSULE · ORAL
Active ingredientsACYCLOVIR (200 mg/1)
Marketing started20140602
Package count2

External sources

Source: openFDA. Public-domain (CC0).