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Fosinopril Sodium - 0093-7223-10 - (Fosinopril Sodium)

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Drug Information of Fosinopril Sodium

Product NDC: 0093-7223
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: 0093-7223
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076139
Marketing Category: ANDA
Start Marketing Date: 20031201

Package Information of Fosinopril Sodium

Package NDC: 0093-7223-10
Package Description: 1000 TABLET in 1 BOTTLE (0093-7223-10)

NDC Information of Fosinopril Sodium

NDC Code 0093-7223-10
Proprietary Name Fosinopril Sodium
Package Description 1000 TABLET in 1 BOTTLE (0093-7223-10)
Product NDC 0093-7223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031201
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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


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