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Fosinopril Sodium - 65862-472-99 - (Fosinopril Sodium)

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Drug Information of Fosinopril Sodium

Product NDC: 65862-472
Proprietary Name: Fosinopril Sodium
Non Proprietary Name: Fosinopril Sodium
Active Ingredient(s): 20    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: 65862-472
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091163
Marketing Category: ANDA
Start Marketing Date: 20110330

Package Information of Fosinopril Sodium

Package NDC: 65862-472-99
Package Description: 1000 TABLET in 1 BOTTLE (65862-472-99)

NDC Information of Fosinopril Sodium

NDC Code 65862-472-99
Proprietary Name Fosinopril Sodium
Package Description 1000 TABLET in 1 BOTTLE (65862-472-99)
Product NDC 65862-472
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110330
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name FOSINOPRIL SODIUM
Strength Number 20
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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