# Diltiazem Hydrochloride

NDC: 47335-679
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20111031

FDA application: ANDA090492

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 360 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-679"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-679
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f71ba5e-7bd6-409a-80c6-2f22d975aefc