| NDC Code | 68210-4120-2 |
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| Package Description | 1 BOTTLE in 1 CARTON (68210-4120-2) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
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| Product NDC | 68210-4120 |
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| Product Type Name | HUMAN OTC 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 | 20200323 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207612 |
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| Manufacturer | Spirit Pharmaceuticals LLC |
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| Substance Name | NAPROXEN SODIUM |
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| Strength | 220 |
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| Strength Unit | 1/1 |
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| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
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