| NDC Code | 51660-423-21 |
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| Package Description | 20 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-21) |
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| Product NDC | 51660-423 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Ibuprofen And Pseudoephedrine Hydrochloride |
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| Non-Proprietary Name | Ibuprofen And Pseudoephedrine Hydrochloride |
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| Dosage Form | TABLET, SUGAR COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20011013 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074567 |
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| Manufacturer | Ohm Laboratories Inc. |
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| Substance Name | IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
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| Strength | 200; 30 |
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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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