# diltiazem hydrochloride

NDC: 50742-252
Generic name: diltiazem hydrochloride
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190614

FDA application: ANDA208783

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 360 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-252"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-252
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=355f560a-8ebb-4661-ad74-2a22f707d7f8