# Diltiazem Hydrochloride Extended-Release

NDC: 10370-830
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20151001

FDA application: ANDA074984

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 180 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10370-830"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10370-830
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a66ad880-cdab-435a-a6f2-574cfdfd1ac3