Product NDC: | 49349-955 |
Proprietary Name: | Diclofenac Potassium |
Non Proprietary Name: | Diclofenac Potassium |
Active Ingredient(s): | 50 mg/1 & nbsp; Diclofenac Potassium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-955 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075219 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120330 |
Package NDC: | 49349-955-03 |
Package Description: | 20 TABLET in 1 BLISTER PACK (49349-955-03) |
NDC Code | 49349-955-03 |
Proprietary Name | Diclofenac Potassium |
Package Description | 20 TABLET in 1 BLISTER PACK (49349-955-03) |
Product NDC | 49349-955 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diclofenac Potassium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120330 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | DICLOFENAC POTASSIUM |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |