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Moexipril Hydrochloride - 60505-0271-1 - (Moexipril Hydrochloride)

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Drug Information of Moexipril Hydrochloride

Product NDC: 60505-0271
Proprietary Name: Moexipril Hydrochloride
Non Proprietary Name: Moexipril Hydrochloride
Active Ingredient(s): 7.5    mg/1 & nbsp;   Moexipril Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Moexipril Hydrochloride

Product NDC: 60505-0271
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078454
Marketing Category: ANDA
Start Marketing Date: 20080609

Package Information of Moexipril Hydrochloride

Package NDC: 60505-0271-1
Package Description: 100 TABLET in 1 BOTTLE (60505-0271-1)

NDC Information of Moexipril Hydrochloride

NDC Code 60505-0271-1
Proprietary Name Moexipril Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (60505-0271-1)
Product NDC 60505-0271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Moexipril Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080609
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name MOEXIPRIL HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Moexipril Hydrochloride


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