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Perindopril Erbumine - 0054-0111-25 - (Perindopril Erbumine)

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Drug Information of Perindopril Erbumine

Product NDC: 0054-0111
Proprietary Name: Perindopril Erbumine
Non Proprietary Name: Perindopril Erbumine
Active Ingredient(s): 4    mg/1 & nbsp;   Perindopril Erbumine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Perindopril Erbumine

Product NDC: 0054-0111
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090072
Marketing Category: ANDA
Start Marketing Date: 20091110

Package Information of Perindopril Erbumine

Package NDC: 0054-0111-25
Package Description: 100 TABLET in 1 BOTTLE (0054-0111-25)

NDC Information of Perindopril Erbumine

NDC Code 0054-0111-25
Proprietary Name Perindopril Erbumine
Package Description 100 TABLET in 1 BOTTLE (0054-0111-25)
Product NDC 0054-0111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Perindopril Erbumine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091110
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc.
Substance Name PERINDOPRIL ERBUMINE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Perindopril Erbumine


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