Quinapril - 65862-619-78 - (Quinapril Hydrochloride)

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Drug Information of Quinapril

Product NDC: 65862-619
Proprietary Name: Quinapril
Non Proprietary Name: Quinapril Hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   Quinapril Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril

Product NDC: 65862-619
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202725
Marketing Category: ANDA
Start Marketing Date: 20130429

Package Information of Quinapril

Package NDC: 65862-619-78
Package Description: 10 BLISTER PACK in 1 CARTON (65862-619-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-619-10)

NDC Information of Quinapril

NDC Code 65862-619-78
Proprietary Name Quinapril
Package Description 10 BLISTER PACK in 1 CARTON (65862-619-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-619-10)
Product NDC 65862-619
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130429
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name QUINAPRIL HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Quinapril


General Information