| NDC Code | 55289-166-20 |
|---|
| Package Description | 20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55289-166-20) |
|---|
| Product NDC | 55289-166 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diclofenac Sodium |
|---|
| Non-Proprietary Name | Diclofenac Sodium |
|---|
| Dosage Form | TABLET, DELAYED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19950928 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074376 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | DICLOFENAC SODIUM |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|