NDC Code | 0363-2389-62 |
Package Description | 4 BLISTER PACK in 1 CARTON (0363-2389-62) / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 0363-2389 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Mucus Relief D |
Non-Proprietary Name | Guaifenesin, Pseudoephedrine Hydrochloride |
Dosage Form | TABLET, MULTILAYER, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20240326 |
Marketing Category Name | ANDA |
Application Number | ANDA214407 |
Manufacturer | Walgreen Company |
Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 1200; 120 |
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] |