"21695-701-16" National Drug Code (NDC)

NDC Code	21695-701-16
Package Description	473 mL in 1 BOTTLE (21695-701-16)
Product NDC	21695-701
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	19971229
Marketing Category Name	ANDA
Application Number	ANDA074650
Manufacturer	Rebel Distributors Corp
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]