Diclofenac Sodium (Page 7 of 7)

75 mg Label

Diclofenac Sodium Delayed-Release Tablets, USP 75mg
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NDC 70882-115-30

Diclofenac Sodium

Delayed-release

Tablets, USP

75 mg

ATTENTION: DISPENSE

WITH MEDICATION GUIDE.

Rx only

30 Enteric-Coated Tablets

DICLOFENAC SODIUM
diclofenac sodium tablet, delayed release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70882-115(NDC:0781-1789)
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
CARNAUBA WAX
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
GLYCERYL MONOSTEARATE
HYDROXYPROPYL CELLULOSE (TYPE H)
HYPROMELLOSES
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
METHACRYLIC ACID — ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
POLYETHYLENE GLYCOLS
POVIDONE
SHELLAC
TITANIUM DIOXIDE
Product Characteristics
Color PINK Score no score
Shape ROUND Size 10mm
Flavor Imprint Code GG739
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70882-115-30 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074394 11/30/1995
Labeler — Cambridge Therapeutics Technologies, LLC (080072003)

Revised: 12/2016 Cambridge Therapeutics Technologies, LLC

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