| NDC Code | 70332-320-01 |
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| Package Description | 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, UNIT-DOSE (70332-320-01) |
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| Product NDC | 70332-320 |
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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 | 20170803 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091134 |
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| Manufacturer | California Pharmaceuticals, LLC |
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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 | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
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