# Diltiazem Hydrochloride Extended-Release

NDC: 60687-217
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170321

FDA application: ANDA074984

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 240 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-217"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-217
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=11b43a17-8038-462b-8902-259431ad5256