# Diltiazem Hydrochloride

NDC: 0615-8032
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19951222

FDA application: ANDA074185

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8032"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8032
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74620be9-5120-491a-a171-e50612c06541