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Sulfamethoxazole and Trimethoprim - 17856-0823-2 - (Sulfamethoxazole and Trimethoprim)

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Drug Information of Sulfamethoxazole and Trimethoprim

Product NDC: 17856-0823
Proprietary Name: Sulfamethoxazole and Trimethoprim
Non Proprietary Name: Sulfamethoxazole and Trimethoprim
Active Ingredient(s): 200; 40    mg/5mL; mg/5mL & nbsp;   Sulfamethoxazole and Trimethoprim
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfamethoxazole and Trimethoprim

Product NDC: 17856-0823
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074650
Marketing Category: ANDA
Start Marketing Date: 19971229

Package Information of Sulfamethoxazole and Trimethoprim

Package NDC: 17856-0823-2
Package Description: 20 mL in 1 CUP (17856-0823-2)

NDC Information of Sulfamethoxazole and Trimethoprim

NDC Code 17856-0823-2
Proprietary Name Sulfamethoxazole and Trimethoprim
Package Description 20 mL in 1 CUP (17856-0823-2)
Product NDC 17856-0823
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfamethoxazole and Trimethoprim
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 19971229
Marketing Category Name ANDA
Labeler Name Atlantic Biologicals Corps
Substance Name SULFAMETHOXAZOLE; TRIMETHOPRIM
Strength Number 200; 40
Strength Unit mg/5mL; mg/5mL
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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