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ENALAPRIL MALEATE - 55648-926-02 - (ENALAPRIL MALEATE)

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Drug Information of ENALAPRIL MALEATE

Product NDC: 55648-926
Proprietary Name: ENALAPRIL MALEATE
Non Proprietary Name: ENALAPRIL MALEATE
Active Ingredient(s): 20    mg/1 & nbsp;   ENALAPRIL MALEATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ENALAPRIL MALEATE

Product NDC: 55648-926
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075483
Marketing Category: ANDA
Start Marketing Date: 20091211

Package Information of ENALAPRIL MALEATE

Package NDC: 55648-926-02
Package Description: 100 TABLET in 1 BOTTLE (55648-926-02)

NDC Information of ENALAPRIL MALEATE

NDC Code 55648-926-02
Proprietary Name ENALAPRIL MALEATE
Package Description 100 TABLET in 1 BOTTLE (55648-926-02)
Product NDC 55648-926
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRIL MALEATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091211
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
Substance Name ENALAPRIL MALEATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ENALAPRIL MALEATE


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