| NDC Code | 58602-832-83 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (58602-832-83) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 58602-832 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Naproxen Sodium And Pseudoephedrine Hydrochloride Sinus And Headache |
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| Non-Proprietary Name | Naproxen Sodium And Pseudoephedrine Hydrochloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20220601 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211360 |
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| Manufacturer | Aurohealth LLC |
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| Substance Name | NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE |
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| Strength | 220; 120 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC] |
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