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Sulfamethoxazole and Trimethoprim - 21695-125-40 - (Sulfamethoxazole and Trimethoprim)

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Drug Information of Sulfamethoxazole and Trimethoprim

Product NDC: 21695-125
Proprietary Name: Sulfamethoxazole and Trimethoprim
Non Proprietary Name: Sulfamethoxazole and Trimethoprim
Active Ingredient(s): 800; 160    mg/1; mg/1 & nbsp;   Sulfamethoxazole and Trimethoprim
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfamethoxazole and Trimethoprim

Product NDC: 21695-125
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076899
Marketing Category: ANDA
Start Marketing Date: 20100225

Package Information of Sulfamethoxazole and Trimethoprim

Package NDC: 21695-125-40
Package Description: 40 TABLET in 1 BOTTLE (21695-125-40)

NDC Information of Sulfamethoxazole and Trimethoprim

NDC Code 21695-125-40
Proprietary Name Sulfamethoxazole and Trimethoprim
Package Description 40 TABLET in 1 BOTTLE (21695-125-40)
Product NDC 21695-125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfamethoxazole and Trimethoprim
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100225
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name SULFAMETHOXAZOLE; TRIMETHOPRIM
Strength Number 800; 160
Strength Unit mg/1; mg/1
Pharmaceutical Classes Sulfonamide Antimicrobial [EPC],Sulfonamides [Chemical/Ingredient],Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA]

Complete Information of Sulfamethoxazole and Trimethoprim


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