# Diltiazem Hydrochloride Extended-Release

NDC: 63629-2159
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20151001

FDA application: ANDA074984

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-2159"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2159
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6cc3b99-2c0f-4d8a-8393-ec042ed7c892