FDA NDC Directory · JSON-LD · Markdown

CHLORDIAZEPOXIDE HYDROCHLORIDE

NDC 42806-565 · HUMAN PRESCRIPTION DRUG · CAPSULE, GELATIN COATED

Labeler / ManufacturerEpic Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA085472
Dosage form / routeCAPSULE, GELATIN COATED · ORAL
Active ingredientsCHLORDIAZEPOXIDE HYDROCHLORIDE (10 mg/1)
Marketing started20210813
Package count1

External sources

Source: openFDA. Public-domain (CC0).