VERAPAMIL HYDROCHLORIDE- verapamil hydrochloride tablet, extended release

verapamil hydrochloride by

Drug Labeling and Warnings

verapamil hydrochloride by is a Prescription medication manufactured, distributed, or labeled by Northwind Pharmaceuticals, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

NDC: 51655-956-52

MFG: 68462-260-05

Verapamil Hydrohloride ER 240 MG

30 tablets

RX only

Lot#: NW08220001

Exp. Date: 02/2016

Each extended release tablet film-coated tablet contains verapamil hydrochloride USP 240mg.

Dosage: See package insert

Store at 68 to 77 degrees F.  Protect from light and moisture.

Store in a tight, light-resistant container (See USP).  Keep out of the reach of children.

Mfg by: Glenmark Generics Ltd India for Glenmark Generics Inc, NJ USA Lot# 02140734

Repackaged by: Northwind Pharmaceuticals, Indianapolis, IN 46256

WARNINGS AND PRECAUTIONS

INGREDIENTS AND APPEARANCE

VERAPAMIL HYDROCHLORIDE 
verapamil hydrochloride tablet, extended release

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 51655-956(NDC:68462-260)
Route of Administration	oral

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29)	VERAPAMIL HYDROCHLORIDE	240 mg  in 30

Product Characteristics
Color	brown	Score	no score
Shape	OVAL	Size	19mm
Flavor		Imprint Code	G74
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51655-956-52	30 in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA078906	05/27/2014

Labeler - Northwind Pharmaceuticals (036986393)

Registrant - Northwind Pharmaceuticals (036986393)

Establishment
Name	Address	ID/FEI	Business Operations
Northwind Pharmaceuticals		036986393	repack(51655-956)