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Fosinopril Sodium - 68462-367-05 - (Fosinopril Sodium)

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Drug Information of Fosinopril Sodium

Product NDC: 68462-367
Proprietary Name: Fosinopril Sodium
Non Proprietary Name: Fosinopril Sodium
Active Ingredient(s): 10    mg/1 & nbsp;   Fosinopril Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fosinopril Sodium

Product NDC: 68462-367
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077222
Marketing Category: ANDA
Start Marketing Date: 20100621

Package Information of Fosinopril Sodium

Package NDC: 68462-367-05
Package Description: 500 TABLET in 1 BOTTLE (68462-367-05)

NDC Information of Fosinopril Sodium

NDC Code 68462-367-05
Proprietary Name Fosinopril Sodium
Package Description 500 TABLET in 1 BOTTLE (68462-367-05)
Product NDC 68462-367
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100621
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name FOSINOPRIL SODIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Fosinopril Sodium


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