| NDC Code | 50742-278-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50742-278-01) |
|---|
| Product NDC | 50742-278 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diclofenac Sodium |
|---|
| Non-Proprietary Name | Diclofenac Sodium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220926 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA216275 |
|---|
| Manufacturer | Ingenus Pharmaceuticals, LLC |
|---|
| Substance Name | DICLOFENAC SODIUM |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|