"70518-2083-0" National Drug Code (NDC)

NDC Code	70518-2083-0
Package Description	200 mL in 1 BOTTLE (70518-2083-0)
Product NDC	70518-2083
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sulfamethoxazole And Trimethoprim
Non-Proprietary Name	Sulfamethoxazole And Trimethoprim
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20190515
Marketing Category Name	ANDA
Application Number	ANDA091348
Manufacturer	REMEDYREPACK INC.
Substance Name	SULFAMETHOXAZOLE; TRIMETHOPRIM
Strength	200; 40
Strength Unit	mg/5mL; mg/5mL
Pharmacy Classes	Sulfonamide Antimicrobial [EPC],Sulfonamides [CS],Cytochrome P450 2C9 Inhibitors [MoA],Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA],Cytochrome P450 2C8 Inhibitors [MoA],Organic Cation Transporter 2 Inhibitors [MoA]