# verapamil hydrochloride

NDC: 68788-6328
Generic name: verapamil hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20161017

FDA application: ANDA090700

## Active ingredients

- VERAPAMIL HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-6328"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-6328
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d23c757d-39f8-48c3-ba63-df2cbe58c516