"70518-2604-1" National Drug Code (NDC)

NDC Code	70518-2604-1
Package Description	20 TABLET in 1 BOTTLE, PLASTIC (70518-2604-1)
Product NDC	70518-2604
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	20200228
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	Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Dihydrofolate Reductase Inhibitor Antibacterial [EPC], Dihydrofolate Reductase Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], Sulfonamide Antimicrobial [EPC], Sulfonamides [CS]