| NDC Code | 0363-0134-78 | 
|---|
			| Package Description | 2 BLISTER PACK in 1 CARTON (0363-0134-78)  / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 
|---|
			| Product NDC | 0363-0134 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Guaifenesin And Pseudoephedrine Hcl | 
|---|
			
			| Non-Proprietary Name | Guaifenesin And Pseudoephedrine Hcl | 
|---|
			| Dosage Form | TABLET, EXTENDED RELEASE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20200805 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA213203 | 
|---|
			| Manufacturer | WALGREEN CO. | 
|---|
			| 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] | 
|---|