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Fosinopril Sodium - 35356-961-90 - (Fosinopril Sodium)

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Drug Information of Fosinopril Sodium

Product NDC: 35356-961
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: 35356-961
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076483
Marketing Category: ANDA
Start Marketing Date: 20040423

Package Information of Fosinopril Sodium

Package NDC: 35356-961-90
Package Description: 90 TABLET in 1 BOTTLE (35356-961-90)

NDC Information of Fosinopril Sodium

NDC Code 35356-961-90
Proprietary Name Fosinopril Sodium
Package Description 90 TABLET in 1 BOTTLE (35356-961-90)
Product NDC 35356-961
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040423
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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