# Verapamil Hydrochloride

NDC: 0378-6320
Generic name: verapamil hydrochloride
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 19990520

FDA application: ANDA075138

## 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:"0378-6320"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-6320
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c86084bc-33aa-eece-5a96-6c0dad2d1a32