# Verapamil Hydrochloride

NDC: 63629-8842
Generic name: verapamil hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, DELAYED RELEASE PELLETS
Routes: ORAL
Marketing started: 19900529
Marketing ended: 20260831
FDA application: NDA019614

## Active ingredients

- VERAPAMIL HYDROCHLORIDE: 360 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-8842"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-8842
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=522bafc3-4352-4840-b296-e399202c4162