# Diltiazem Hydrochloride Extended-Release

NDC: 75907-046
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: Dr. Reddy's Labratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240910

FDA application: ANDA215775

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 120 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75907-046"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75907-046
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1d09c53-5eb9-0b7c-e977-e2a602e84e5f