| NDC Code | 85722-0001-6 | 
|---|
			| Package Description | 473 mL in 1 BOTTLE (85722-0001-6) | 
|---|
			| Product NDC | 85722-0001 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Dextromethorphan Hydrobromide And Guaifenesin | 
|---|
			
			| Non-Proprietary Name | Dextromethorphan Hydrobromide And Guaifenesin | 
|---|
			| Dosage Form | SYRUP | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20210201 | 
|---|
			
			| Marketing Category Name | OTC MONOGRAPH DRUG | 
|---|
			| Application Number | M012 | 
|---|
			| Manufacturer | KJD Pharma Private Limited | 
|---|
			| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN | 
|---|
			| Strength | 10; 100 | 
|---|
			| Strength Unit | mg/5mL; mg/5mL | 
|---|
			| 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] | 
|---|