Home – Ondansetron HCL

Ondansetron HCL

FULL PRESCRIBING INFORMATION

NDC: 51655-400-43

MFG: 63304-458-30

Ondansetron 4 MG

3 Tablets

RX Only

Dosage: See package insert

Store at 68 to 77 degrees F.

Keep out of the reach of children.

Each film-coated tablet contains 5 mg of ondansetron hydrochloride, USP equivalent to 4 mg of ondansetron.

Mfg. by Natco Pharma Ltd. Kothur 509 228 A. P. India for Ranbaxy Pharmaceuticals, Jacksonville FL 33257 Lot # 404048

Repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46256

Lot# NW25310001

Exp Date: 07/2015

Ondansetron HCL

Dosage: see package insert. Store at 68 to 77 degrees F. Keep out of reach of children.

Ondansetron HCL TABLET, COATED

Product Information
Product Type	Human prescription drug label	Item Code (Source)	NDC:51655-400(NDC:63304-458)
Route of Administration	oral	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ONDANSETRON HYDROCHLORIDE ONDANSETRON		4 mg

Product Characteristics
Color	Size	Imprint Code	Shape
white	10 mm	NO;4	OVAL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:51655-400-43	3 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA077851	2014-03-17

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!