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Sulfamethoxazole and Trimethoprim - 49349-665-03 - (Sulfamethoxazle and Trimethoprim)

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Drug Information of Sulfamethoxazole and Trimethoprim

Product NDC: 49349-665
Proprietary Name: Sulfamethoxazole and Trimethoprim
Non Proprietary Name: Sulfamethoxazle and Trimethoprim
Active Ingredient(s): 800; 160    mg/1; mg/1 & nbsp;   Sulfamethoxazle and Trimethoprim
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfamethoxazole and Trimethoprim

Product NDC: 49349-665
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076899
Marketing Category: ANDA
Start Marketing Date: 20110517

Package Information of Sulfamethoxazole and Trimethoprim

Package NDC: 49349-665-03
Package Description: 20 TABLET in 1 BLISTER PACK (49349-665-03)

NDC Information of Sulfamethoxazole and Trimethoprim

NDC Code 49349-665-03
Proprietary Name Sulfamethoxazole and Trimethoprim
Package Description 20 TABLET in 1 BLISTER PACK (49349-665-03)
Product NDC 49349-665
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfamethoxazle and Trimethoprim
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110517
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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