FDA NDC Directory · JSON-LD · Markdown

CHLORDIAZEPOXIDE HYDROCHLORIDE

NDC 42806-564 · HUMAN PRESCRIPTION DRUG · CAPSULE, GELATIN COATED

Labeler / ManufacturerEpic Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA085461
Dosage form / routeCAPSULE, GELATIN COATED · ORAL
Active ingredientsCHLORDIAZEPOXIDE HYDROCHLORIDE (5 mg/1)
Marketing started20211109
Package count1

External sources

Source: openFDA. Public-domain (CC0).