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Sulfamethoxazole and Trimethoprim - 65862-496-01 - (Sulfamethoxazole and Trimethoprim)

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Drug Information of Sulfamethoxazole and Trimethoprim

Product NDC: 65862-496
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: 65862-496
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091348
Marketing Category: ANDA
Start Marketing Date: 20100608

Package Information of Sulfamethoxazole and Trimethoprim

Package NDC: 65862-496-01
Package Description: 100 mL in 1 BOTTLE (65862-496-01)

NDC Information of Sulfamethoxazole and Trimethoprim

NDC Code 65862-496-01
Proprietary Name Sulfamethoxazole and Trimethoprim
Package Description 100 mL in 1 BOTTLE (65862-496-01)
Product NDC 65862-496
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfamethoxazole and Trimethoprim
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20100608
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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