| NDC Code | 68016-222-00 |
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| Package Description | 177 mL in 1 BOTTLE (68016-222-00) |
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| Product NDC | 68016-222 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Dm Max |
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| Proprietary Name Suffix | Maxium Strength |
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| Non-Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20130101 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Chain Drug Consortium, LLC |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
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| Strength | 20; 400 |
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| Strength Unit | mg/20mL; mg/20mL |
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| Pharmacy Classes | 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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