| NDC Code | 50991-736-90 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (50991-736-90) / 90 TABLET in 1 BOTTLE |
|---|
| Product NDC | 50991-736 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Deconex Ir |
|---|
| Non-Proprietary Name | Guaifenesin And Phenylephrine Hcl |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160808 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M012 |
|---|
| Manufacturer | Poly Pharmaceuticals, Inc. |
|---|
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 385; 10 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC] |
|---|