# diltiazem hydrochloride

NDC: 68382-598
Generic name: diltiazem hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170928

FDA application: ANDA206534

## 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:"68382-598"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-598
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1e2f2025-0350-40c4-ab42-3b57f3d105a6