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Fluvastatin Sodium - 0378-8020-93 - (fluvastatin)

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Drug Information of Fluvastatin Sodium

Product NDC: 0378-8020
Proprietary Name: Fluvastatin Sodium
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 Sodium

Product NDC: 0378-8020
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090595
Marketing Category: ANDA
Start Marketing Date: 20130319

Package Information of Fluvastatin Sodium

Package NDC: 0378-8020-93
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (0378-8020-93)

NDC Information of Fluvastatin Sodium

NDC Code 0378-8020-93
Proprietary Name Fluvastatin Sodium
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (0378-8020-93)
Product NDC 0378-8020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluvastatin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130319
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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 Sodium


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