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Verapamil Hydrochloride

NDC 0591-2882 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE PELLETS

Generic nameverapamil hydrochloride
Labeler / ManufacturerTeva Pharmaceuticals Inc
Marketing categoryNew Drug Application (innovator) · App NDA019614
Dosage form / routeCAPSULE, DELAYED RELEASE PELLETS · ORAL
Active ingredientsVERAPAMIL HYDROCHLORIDE (180 mg/1)
Marketing started19900529
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).