| NDC Code | 68151-0738-0 |
|---|
| Package Description | 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (68151-0738-0) |
|---|
| Product NDC | 68151-0738 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Etodolac |
|---|
| Non-Proprietary Name | Etodolac |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20010209 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA075665 |
|---|
| Manufacturer | Carilion Materials Management |
|---|
| Substance Name | ETODOLAC |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|