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