| NDC Code | 0031-8692-13 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (0031-8692-13) / 118 mL in 1 BOTTLE |
|---|
| Product NDC | 0031-8692 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Childrens Robitussin Nighttime Cough Long-acting Dm |
|---|
| Non-Proprietary Name | Chlorpheniramine Maleate, Dextromethorphan Hydrobromide |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140701 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M012 |
|---|
| Manufacturer | Haleon US Holdings LLC |
|---|
| Substance Name | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE |
|---|
| Strength | 2; 15 |
|---|
| Strength Unit | mg/10mL; mg/10mL |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
|---|