| NDC Code | 37808-158-60 |
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| Package Description | 20 BLISTER PACK in 1 CARTON (37808-158-60) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 37808-158 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Congestion Relief |
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| Non-Proprietary Name | Ibuprofen, Phenylephrine Hcl |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20160418 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203200 |
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| Manufacturer | H E B |
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| Substance Name | IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 200; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-1 Adrenergic Agonist [EPC] |
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