# Verapamil Hydrochloride

NDC: 51754-0204
Generic name: Verapamil Hydrochloride
Labeler / Manufacturer: EXELA PHARMA SCIENCES, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20170201

FDA application: NDA018925

## Active ingredients

- VERAPAMIL HYDROCHLORIDE: 2.5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51754-0204"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51754-0204
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3318e357-0660-44f4-8170-91a51bd762fb