| NDC Code | 68016-217-32 |
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| Package Description | 1 BOTTLE in 1 BOX (68016-217-32) > 32 CAPSULE, LIQUID FILLED in 1 BOTTLE |
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| Product NDC | 68016-217 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Ibuprofen And Diphenhydramine Hcl |
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| Non-Proprietary Name | Ibuprofen, Diphenhydramine Hcl |
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| Dosage Form | CAPSULE, LIQUID FILLED |
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| Usage | ORAL |
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| Start Marketing Date | 20130104 |
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| End Marketing Date | 20191231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090397 |
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| Manufacturer | Chain Drug Consortium, LLC |
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| Substance Name | IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 200; 25 |
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| Strength Unit | mg/1; mg/1 |
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