| NDC Code | 37808-733-20 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (37808-733-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 37808-733 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Mucus Relief Dm |
|---|
| Non-Proprietary Name | Guaifenesin, Dextromethorphan Hbr |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20230228 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209692 |
|---|
| Manufacturer | H E B |
|---|
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
|---|
| Strength | 30; 600 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | 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] |
|---|