"70518-1381-1" National Drug Code (NDC)

NDC Code	70518-1381-1
Package Description	20 TABLET in 1 BLISTER PACK (70518-1381-1)
Product NDC	70518-1381
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sulfamethoxazole And Trimethoprim
Non-Proprietary Name	Sulfamethoxazole And Trimethoprim
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20180829
Marketing Category Name	ANDA
Application Number	ANDA090624
Manufacturer	REMEDYREPACK INC.
Substance Name	SULFAMETHOXAZOLE; TRIMETHOPRIM
Strength	800; 160
Strength Unit	mg/1; mg/1
Pharmacy Classes	Sulfonamide Antimicrobial [EPC],Sulfonamides [Chemical/Ingredient],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]