Diclofenac Sodium (Page 5 of 5)

PACKAGE DISPLAY PANEL

Diclofenac bottle label
(click image for full-size original)

DICLOFENAC SODIUM
diclofenac sodium tablet, delayed release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-800(NDC:0228-2551)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
diclofenac sodium (diclofenac) diclofenac sodium 75 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
HYPROMELLOSES
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYSORBATE 80
POLYVINYL ACETATE PHTHALATE
PROPYLENE GLYCOL
SODIUM ALGINATE
STEARIC ACID
FERROSOFERRIC OXIDE
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape ROUND Size 9mm
Flavor Imprint Code 551
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-800-42 60 TABLET, DELAYED RELEASE (TABLET) in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074514 07/01/2011
Labeler — McKesson Packaging Services a business unit of McKesson Corporation (140529962)
Registrant — McKesson Packaging Services a business unit of McKesson Corporation (140529962)
Establishment
Name Address ID/FEI Operations
RxPak Division of McKesson Corporation 177667227 REPACK

Revised: 07/2011 McKesson Packaging Services a business unit of McKesson Corporation

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