| NDC Code | 63868-244-04 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (63868-244-04) / 118 mL in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 63868-244 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Tussin Cf |
|---|
| Proprietary Name Suffix | Non Drowsy |
|---|
| Non-Proprietary Name | Dextromethorphan Hbr, Guaifenesin, Phenylephrine |
|---|
| Dosage Form | LIQUID |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140630 |
|---|
| End Marketing Date | 20241231 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part341 |
|---|
| Manufacturer | QUALITY CHOICE (Chain Drug Marketing Association) |
|---|
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 20; 200; 10 |
|---|
| Strength Unit | mg/10mL; mg/10mL; mg/10mL |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], 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], alpha-1 Adrenergic Agonist [EPC] |
|---|