NDC Code | 65841-778-77 |
Package Description | 100 BLISTER PACK in 1 CARTON (65841-778-77) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65841-778-30) |
Product NDC | 65841-778 |
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 | 20140215 |
Marketing Category Name | ANDA |
Application Number | ANDA091134 |
Manufacturer | Zydus Lifesciences Limited |
Substance Name | ETODOLAC |
Strength | 500 |
Strength Unit | mg/1 |
Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |