| NDC Code | 63868-716-20 |
|---|
| Package Description | 2 BLISTER PACK in 1 CARTON (63868-716-20) > 10 TABLET, COATED in 1 BLISTER PACK |
|---|
| Product NDC | 63868-716 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Mucus Relief Severe Cold |
|---|
| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride |
|---|
| Dosage Form | TABLET, COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130924 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part341 |
|---|
| Manufacturer | Chain Drug Marketing Association |
|---|
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 325; 10; 200; 5 |
|---|
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], 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] |
|---|