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Trandolapril - 0378-3242-05 - (Trandolapril)

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Drug Information of Trandolapril

Product NDC: 0378-3242
Proprietary Name: Trandolapril
Non Proprietary Name: Trandolapril
Active Ingredient(s): 2    mg/1 & nbsp;   Trandolapril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Trandolapril

Product NDC: 0378-3242
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078346
Marketing Category: ANDA
Start Marketing Date: 20100823

Package Information of Trandolapril

Package NDC: 0378-3242-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0378-3242-05)

NDC Information of Trandolapril

NDC Code 0378-3242-05
Proprietary Name Trandolapril
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0378-3242-05)
Product NDC 0378-3242
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trandolapril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100823
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name TRANDOLAPRIL
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Trandolapril


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