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Fluvastatin - 0093-7442-01 - (Fluvastatin)

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Drug Information of Fluvastatin

Product NDC: 0093-7442
Proprietary Name: Fluvastatin
Non Proprietary Name: Fluvastatin
Active Ingredient(s): 20    mg/1 & nbsp;   Fluvastatin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluvastatin

Product NDC: 0093-7442
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078407
Marketing Category: ANDA
Start Marketing Date: 20120705

Package Information of Fluvastatin

Package NDC: 0093-7442-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-7442-01)

NDC Information of Fluvastatin

NDC Code 0093-7442-01
Proprietary Name Fluvastatin
Package Description 100 CAPSULE in 1 BOTTLE (0093-7442-01)
Product NDC 0093-7442
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluvastatin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120705
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name FLUVASTATIN SODIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Fluvastatin


General Information