# Diltiazem hydrochloride

NDC: 72578-202
Generic name: Diltiazem hydrochloride
Labeler / Manufacturer: Viona Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260525

FDA application: ANDA219253

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72578-202"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72578-202
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43cffe12-304a-4e15-9512-94f812188f1a