Product NDC: | 63629-4108 |
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, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-4108 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075219 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100121 |
Package NDC: | 63629-4108-3 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4108-3) |
NDC Code | 63629-4108-3 |
Proprietary Name | Diclofenac Potassium |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4108-3) |
Product NDC | 63629-4108 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diclofenac Potassium |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100121 |
Marketing Category Name | ANDA |
Labeler Name | Bryant Ranch Prepack |
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] |