| NDC Code | 43063-242-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43063-242-30) |
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| Product NDC | 43063-242 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Naprelan |
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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 | 20081219 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020353 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | NAPROXEN SODIUM |
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| Strength | 750 |
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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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