| NDC Code | 69367-272-04 |
|---|
| Package Description | 118 mL in 1 BOTTLE (69367-272-04) |
|---|
| Product NDC | 69367-272 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Codeine-guaifenesin |
|---|
| Non-Proprietary Name | Codeine Phosphate And Guaifenesin |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200715 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M012 |
|---|
| Manufacturer | Westminster Pharmaceuticals, LLC |
|---|
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN |
|---|
| Strength | 10; 100 |
|---|
| Strength Unit | mg/5mL; mg/5mL |
|---|
| Pharmacy Classes | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Full Opioid Agonists [MoA], Increased Respiratory Secretions [PE], Opioid Agonist [EPC] |
|---|
| DEA Schedule | CV |
|---|