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Trimethoprim - 54868-1616-1 - (Trimethoprim)

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Drug Information of Trimethoprim

Product NDC: 54868-1616
Proprietary Name: Trimethoprim
Non Proprietary Name: Trimethoprim
Active Ingredient(s): 100    mg/1 & nbsp;   Trimethoprim
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Trimethoprim

Product NDC: 54868-1616
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070049
Marketing Category: ANDA
Start Marketing Date: 20120502

Package Information of Trimethoprim

Package NDC: 54868-1616-1
Package Description: 30 TABLET in 1 BOTTLE (54868-1616-1)

NDC Information of Trimethoprim

NDC Code 54868-1616-1
Proprietary Name Trimethoprim
Package Description 30 TABLET in 1 BOTTLE (54868-1616-1)
Product NDC 54868-1616
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trimethoprim
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120502
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name TRIMETHOPRIM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA]

Complete Information of Trimethoprim


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