NDC 51655-956 – Verapamil hydrochloride

Verapamil Hydrochloride 240 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC51655-956

Product details

Brand name
Verapamil hydrochloride
Generic name
Verapamil hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078906
Marketed since
May 27, 2014
Listing expires
December 31, 2027
Pharmacologic class
Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Verapamil Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
51655-956-2690 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-956-26)May 18, 2023
51655-956-5230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, DISPENSING (51655-956-52)May 27, 2014

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