| NDC Code | 43063-801-90 |
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| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (43063-801-90) |
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| Product NDC | 43063-801 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Guaifenesin Dm |
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| Non-Proprietary Name | Guaifenesin And Dextromethorphan Hydrobromide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20180402 |
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| End Marketing Date | 20271130 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
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| Strength | 20; 400 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
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