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Enalapril Maleate - 15338-233-30 - (Enalapril Maleate)

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Drug Information of Enalapril Maleate

Product NDC: 15338-233
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, SOLUBLE
Coding System: National Drug Codes(NDC)

Labeler Information of Enalapril Maleate

Product NDC: 15338-233
Labeler Name: Apace Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075843
Marketing Category: ANDA
Start Marketing Date: 20090822

Package Information of Enalapril Maleate

Package NDC: 15338-233-30
Package Description: 12 BOTTLE in 1 CARTON (15338-233-30) > 30 TABLET, SOLUBLE in 1 BOTTLE

NDC Information of Enalapril Maleate

NDC Code 15338-233-30
Proprietary Name Enalapril Maleate
Package Description 12 BOTTLE in 1 CARTON (15338-233-30) > 30 TABLET, SOLUBLE in 1 BOTTLE
Product NDC 15338-233
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enalapril Maleate
Dosage Form Name TABLET, SOLUBLE
Route Name ORAL
Start Marketing Date 20090822
Marketing Category Name ANDA
Labeler Name Apace Packaging
Substance Name ENALAPRIL MALEATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Enalapril Maleate


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