# verapamil hydrochloride

NDC: 55289-723
Generic name: verapamil hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
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:"55289-723"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-723
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3c215e6c-d85a-4102-a1c2-f00fa3169a55