| NDC Code | 55111-565-14 |
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| Package Description | 1 BOTTLE in 1 CARTON (55111-565-14) > 20 TABLET in 1 BOTTLE |
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| Product NDC | 55111-565 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Ibuprofen And Diphenhydramine Citrate |
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| Non-Proprietary Name | Ibuprofen And Diphenhydramine Citrate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20100131 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090619 |
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| Manufacturer | Dr. Reddy's Laboratories Limited |
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| Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
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| Strength | 38; 200 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC] |
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