# Cardizem

NDC: 0187-0771
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: Bausch Health US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20101225

FDA application: NDA018602

## 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:"0187-0771"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0187-0771
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3e7ecef-f360-4987-a4f5-933214130ab2