| NDC Code | 65841-779-10 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-779-10) |
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| Product NDC | 65841-779 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Etodolac |
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| Non-Proprietary Name | Etodolac |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20140215 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091134 |
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| Manufacturer | Zydus Lifesciences Limited |
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| Substance Name | ETODOLAC |
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| Strength | 600 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
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