# CHLORDIAZEPOXIDE HYDROCHLORIDE

NDC: 42806-564
Generic name: CHLORDIAZEPOXIDE HYDROCHLORIDE
Labeler / Manufacturer: Epic Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 20211109

FDA application: ANDA085461

## Active ingredients

- CHLORDIAZEPOXIDE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42806-564"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-564
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e198c16-a929-4028-8f96-25dd23f74b10