NDC Code | 50742-279-01 |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50742-279-01) |
Product NDC | 50742-279 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diclofenac Potassium |
Non-Proprietary Name | Diclofenac Potassium |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20211011 |
Marketing Category Name | ANDA |
Application Number | ANDA215585 |
Manufacturer | Ingenus Pharmaceuticals, LLC |
Substance Name | DICLOFENAC POTASSIUM |
Strength | 50 |
Strength Unit | mg/1 |
Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC] |