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FOSINOPRIL Na - 60505-2512-3 - (FOSINOPRIL Sodium)

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Drug Information of FOSINOPRIL Na

Product NDC: 60505-2512
Proprietary Name: FOSINOPRIL Na
Non Proprietary Name: FOSINOPRIL Sodium
Active Ingredient(s): 40    mg/1 & nbsp;   FOSINOPRIL Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FOSINOPRIL Na

Product NDC: 60505-2512
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076906
Marketing Category: ANDA
Start Marketing Date: 20050518

Package Information of FOSINOPRIL Na

Package NDC: 60505-2512-3
Package Description: 100 TABLET in 1 BOTTLE (60505-2512-3)

NDC Information of FOSINOPRIL Na

NDC Code 60505-2512-3
Proprietary Name FOSINOPRIL Na
Package Description 100 TABLET in 1 BOTTLE (60505-2512-3)
Product NDC 60505-2512
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FOSINOPRIL Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050518
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name FOSINOPRIL SODIUM
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of FOSINOPRIL Na


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