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Trandolapril - 0378-3241-01 - (Trandolapril)

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Drug Information of Trandolapril

Product NDC: 0378-3241
Proprietary Name: Trandolapril
Non Proprietary Name: Trandolapril
Active Ingredient(s): 1    mg/1 & nbsp;   Trandolapril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Trandolapril

Product NDC: 0378-3241
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: 0378-3241-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-3241-01)

NDC Information of Trandolapril

NDC Code 0378-3241-01
Proprietary Name Trandolapril
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-3241-01)
Product NDC 0378-3241
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 1
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Trandolapril


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