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Moexipril Hydrochloride - 54868-4883-1 - (Moexipril Hydrochloride)

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Drug Information of Moexipril Hydrochloride

Product NDC: 54868-4883
Proprietary Name: Moexipril Hydrochloride
Non Proprietary Name: Moexipril Hydrochloride
Active Ingredient(s): 15    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: 54868-4883
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078454
Marketing Category: ANDA
Start Marketing Date: 20040427

Package Information of Moexipril Hydrochloride

Package NDC: 54868-4883-1
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (54868-4883-1)

NDC Information of Moexipril Hydrochloride

NDC Code 54868-4883-1
Proprietary Name Moexipril Hydrochloride
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (54868-4883-1)
Product NDC 54868-4883
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Moexipril Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040427
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name MOEXIPRIL HYDROCHLORIDE
Strength Number 15
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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