| NDC Code | 80425-0457-3 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0457-3) |
|---|
| Product NDC | 80425-0457 |
|---|
| 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 | 20241021 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA215787 |
|---|
| Manufacturer | Advanced Rx of Tennessee, 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] |
|---|