| NDC Code | 70000-0171-2 |
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| Package Description | 1 BOTTLE in 1 CARTON (70000-0171-2) > 200 TABLET, FILM COATED in 1 BOTTLE |
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| Product NDC | 70000-0171 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Leader All Day Pain Relief |
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| Non-Proprietary Name | Naproxen Sodium |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20161129 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074661 |
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| Manufacturer | Cardinal Health 110, LLC. dba Leader |
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| Substance Name | NAPROXEN SODIUM |
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| Strength | 220 |
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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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