Home > National Drug Code (NDC) > Fosinopril Sodium

Fosinopril Sodium - 60429-756-45 - (Fosinopril Sodium)

Alphabetical Index


Drug Information of Fosinopril Sodium

Product NDC: 60429-756
Proprietary Name: Fosinopril Sodium
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 Sodium

Product NDC: 60429-756
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077222
Marketing Category: ANDA
Start Marketing Date: 20100621

Package Information of Fosinopril Sodium

Package NDC: 60429-756-45
Package Description: 45 TABLET in 1 BOTTLE (60429-756-45)

NDC Information of Fosinopril Sodium

NDC Code 60429-756-45
Proprietary Name Fosinopril Sodium
Package Description 45 TABLET in 1 BOTTLE (60429-756-45)
Product NDC 60429-756
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 Golden State Medical Supply, Inc.
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 Sodium


General Information