NDC Code | 51660-073-86 |
Package Description | 2 BLISTER PACK in 1 CARTON (51660-073-86) > 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 51660-073 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Guaifenesin And Dextromethorphan Hydrobromide |
Non-Proprietary Name | Guaifenesin And Dextromethorphan Hydrobromide |
Dosage Form | TABLET, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20171210 |
Marketing Category Name | NDA |
Application Number | NDA021620 |
Manufacturer | OHM LABORATORIES INC |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength | 60; 1200 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |