| NDC Code | 0113-8911-62 | 
|---|
			| Package Description | 4 BLISTER PACK in 1 CARTON (0113-8911-62)  / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK | 
|---|
			| Product NDC | 0113-8911 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Mucus D | 
|---|
			
			| Non-Proprietary Name | Guaifenesin, Pseudoephedrine Hydrochloride | 
|---|
			| Dosage Form | TABLET, MULTILAYER, EXTENDED RELEASE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20251003 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA214407 | 
|---|
			| Manufacturer | L. Perrigo 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] | 
|---|