| NDC Code | 50844-292-13 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-13) / 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
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| Product NDC | 50844-292 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Ibuprofen |
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| Non-Proprietary Name | Ibuprofen |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 19880524 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075010 |
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| Manufacturer | L.N.K. International, Inc. |
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| Substance Name | IBUPROFEN |
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| Strength | 200 |
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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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