Zipsor - 13913-008-94 - (diclofenac potassium)

Alphabetical Index


Drug Information of Zipsor

Product NDC: 13913-008
Proprietary Name: Zipsor
Non Proprietary Name: diclofenac potassium
Active Ingredient(s): 25    mg/1 & nbsp;   diclofenac potassium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Zipsor

Product NDC: 13913-008
Labeler Name: Depomed, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022202
Marketing Category: NDA
Start Marketing Date: 20100430

Package Information of Zipsor

Package NDC: 13913-008-94
Package Description: 1 BLISTER PACK in 1 CARTON (13913-008-94) > 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Zipsor

NDC Code 13913-008-94
Proprietary Name Zipsor
Package Description 1 BLISTER PACK in 1 CARTON (13913-008-94) > 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 13913-008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diclofenac potassium
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20100430
Marketing Category Name NDA
Labeler Name Depomed, Inc.
Substance Name DICLOFENAC POTASSIUM
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Zipsor


General Information