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Moexipril Hydrochloride - 0093-0017-01 - (Moexipril Hydrochloride)

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Drug Information of Moexipril Hydrochloride

Product NDC: 0093-0017
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Moexipril Hydrochloride

Product NDC: 0093-0017
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076204
Marketing Category: ANDA
Start Marketing Date: 20030508

Package Information of Moexipril Hydrochloride

Package NDC: 0093-0017-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)

NDC Information of Moexipril Hydrochloride

NDC Code 0093-0017-01
Proprietary Name Moexipril Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)
Product NDC 0093-0017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Moexipril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030508
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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