| NDC Code | 71269-040-30 |
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| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71269-040-30) |
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| Product NDC | 71269-040 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tuxarin |
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| Non-Proprietary Name | Codeine Phosphate And Chlorpheniramine Maleate |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20181015 |
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| Marketing Category Name | NDA |
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| Application Number | NDA206323 |
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| Manufacturer | Mainpointe Pharmaceuticals |
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| Substance Name | CHLORPHENIRAMINE MALEATE; CODEINE PHOSPHATE |
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| Strength | 8; 54.3 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Full Opioid Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Opioid Agonist [EPC] |
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| DEA Schedule | CIII |
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