| NDC Code | 52959-649-15 |
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| Package Description | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 VIAL (52959-649-15) |
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| Product NDC | 52959-649 |
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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 | 20170306 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091134 |
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| Manufacturer | H.J. HARKINS COMPANY, INC. |
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| Substance Name | ETODOLAC |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
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