| NDC Code | 60687-651-21 |
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| Package Description | 30 BLISTER PACK in 1 CARTON (60687-651-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-651-11) |
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| Product NDC | 60687-651 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Mucinex Dm |
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| Non-Proprietary Name | Guaifenesin And Dextromethorphan Hydrobromide |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20220714 |
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| End Marketing Date | 20240229 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021620 |
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| Manufacturer | American Health Packaging |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
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| Strength | 30; 600 |
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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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