# DILTIAZEM HYDROCHLORIDE

NDC: 50228-498
Generic name: diltiazem hydrochloride
Labeler / Manufacturer: ScieGen Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230406

FDA application: ANDA216327

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50228-498"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50228-498
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1ca03c9e-edc8-4c7f-89ee-f2346ea8c067