# Diltiazem Hydrochloride

NDC: 62135-335
Generic name: Diltiazem Hydrochloride
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19921105

FDA application: ANDA074093

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 90 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-335"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-335
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51abce7b-e3d1-44b5-bccc-d463150d0bba
