# Verapamil Hydrochloride

NDC: 70771-1601
Generic name: Verapamil Hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20201022

FDA application: ANDA214215

## Active ingredients

- VERAPAMIL HYDROCHLORIDE: 2.5 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1601"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1601
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cccf4a5f-6c5d-4d52-97e4-fe7a2dbd28d8