NDC Code | 0363-1604-37 |
Package Description | 2 BLISTER PACK in 1 CARTON (0363-1604-37) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 0363-1604 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Mucus Relief D |
Non-Proprietary Name | Guaifenesin And Pseudoephedrine Hcl |
Dosage Form | TABLET, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20190813 |
Marketing Category Name | ANDA |
Application Number | ANDA208369 |
Manufacturer | Walgreens Company |
Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 600; 60 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC] |