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Fosinopril Sodium - 31722-201-90 - (Fosinopril Sodium)

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Drug Information of Fosinopril Sodium

Product NDC: 31722-201
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: 31722-201
Labeler Name: Camber Pharmceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077222
Marketing Category: ANDA
Start Marketing Date: 20070917

Package Information of Fosinopril Sodium

Package NDC: 31722-201-90
Package Description: 90 TABLET in 1 BOTTLE (31722-201-90)

NDC Information of Fosinopril Sodium

NDC Code 31722-201-90
Proprietary Name Fosinopril Sodium
Package Description 90 TABLET in 1 BOTTLE (31722-201-90)
Product NDC 31722-201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070917
Marketing Category Name ANDA
Labeler Name Camber Pharmceuticals Inc.
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


General Information