# Diltiazem Hydrochloride

NDC: 68682-993
Generic name: Diltiazem hydrochloride
Labeler / Manufacturer: OCEANSIDE PHARMACEUTICALS
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 19991228

FDA application: ANDA075116

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 120 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68682-993"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68682-993
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43892b97-449d-45bc-bb09-29d47c655d65