Valsartan (Page 6 of 6)

Package Label.Principal Display

NDC: 51655-751-52

MFG NDC: 51600-142-90

Valsartan 160mg

30 Tablets

Rx Only

Lot: NW48320001

Exp Date: 10/2015

Each film-caoted tablet contains 160mg of valsartan, USP

Dosage: See prescriber’s instructions

Store between 68-77 degrees F. protect from moisture.

Keep out of the reach of children.

Medication guide is found at www.fda.gov/drugs/drugsafety/ucm085729

Dist. by Ohm Laboratories, Inc. North Brunswick, NJ 08902 Lot# 2568187

Repackaged by: Northwind Pharmaceuticals, Indianapolis, IN 46256

51655075152
(click image for full-size original)
VALSARTAN
valsartan tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-751(NDC:51660-142)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VALSARTAN (VALSARTAN) VALSARTAN 160 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
CROSPOVIDONE
HYPROMELLOSES
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
STARCH, CORN
TALC
TITANIUM DIOXIDE
FERRIC OXIDE RED
FERROSOFERRIC OXIDE
POLYETHYLENE GLYCOLS
Product Characteristics
Color pink Score no score
Shape OVAL Size 15mm
Flavor Imprint Code RX125
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51655-751-52 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077492 01/07/2015
Labeler — Northwind Pharmaceuticals (036986393)
Registrant — Northwind Pharmaceuticals (036986393)
Establishment
Name Address ID/FEI Operations
Northwind Pharmaceuticals 036986393 repack (51655-751)

Revised: 04/2015 Northwind Pharmaceuticals

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