# VERAPAMIL HYDROCHLORIDE

NDC: 51655-734
Generic name: VERAPAMIL HYDROCHLORIDE
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210617

FDA application: ANDA206173

## Active ingredients

- VERAPAMIL HYDROCHLORIDE: 180 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-734"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-734
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db990ce1-b193-4a81-e053-2a95a90a627b