NDC Code | 71337-046-05 |
Package Description | 500 TABLET in 1 BOTTLE (71337-046-05) |
Product NDC | 71337-046 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diclofenac Potassium |
Non-Proprietary Name | Diclofenac Potassium, Film Coated |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20230625 |
Marketing Category Name | ANDA |
Application Number | ANDA215787 |
Manufacturer | Havix Group Inc d-b-a Aavis Pharmaceuticals |
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] |