# Diltiazem Hydrochloride

NDC: 0409-4350
Generic name: DILTIAZEM HYDROCHLORIDE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20050430

FDA application: ANDA075853

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-4350"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-4350
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bba03666-ff4f-4bf6-fa92-78e1ec2d9073