| NDC Code | 35356-867-30 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (35356-867-30) |
|---|
| Product NDC | 35356-867 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diclofenac Sodium |
|---|
| Non-Proprietary Name | Diclofenac Sodium |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19960308 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020254 |
|---|
| Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
|---|
| Substance Name | DICLOFENAC SODIUM |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|