| NDC Code | 62037-826-75 |
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| Package Description | 75 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-826-75) |
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| Product NDC | 62037-826 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Naproxen Sodium |
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| Non-Proprietary Name | Naproxen Sodium |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20140930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075416 |
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| Manufacturer | Actavis Pharma, Inc. |
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| Substance Name | NAPROXEN SODIUM |
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| Strength | 500 |
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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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