# verapamil hydrochloride

NDC: 71205-017
Generic name: verapamil hydrochloride
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20090917

FDA application: ANDA078906

## Active ingredients

- VERAPAMIL HYDROCHLORIDE: 240 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-017"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-017
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4ffa579e-1d85-4b3b-ae06-6a9334e0f9e1