NDC Code | 80425-0381-1 |
Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (80425-0381-1) |
Product NDC | 80425-0381 |
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 | 20240410 |
Marketing Category Name | ANDA |
Application Number | ANDA091134 |
Manufacturer | Advanced Rx Pharmacy of Tennessee, LLC |
Substance Name | ETODOLAC |
Strength | 600 |
Strength Unit | mg/1 |
Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |