NDC 0527-2580

Fluvastatin Sodium

Fluvastatin Sodium

Fluvastatin Sodium is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Lannett Company, Inc.. The primary component is Fluvastatin Sodium.

Product ID0527-2580_c1be7832-b98b-d8fb-e053-2995a90a9b83
NDC0527-2580
Product TypeHuman Prescription Drug
Proprietary NameFluvastatin Sodium
Generic NameFluvastatin Sodium
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2021-05-07
Marketing CategoryANDA /
Application NumberANDA209397
Labeler NameLannett Company, Inc.
Substance NameFLUVASTATIN SODIUM
Active Ingredient Strength80 mg/1
Pharm ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0527-2580-32

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0527-2580-32)
Marketing Start Date2021-05-07
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Fluvastatin Sodium" or generic name "Fluvastatin Sodium"

NDCBrand NameGeneric Name
0093-7446Fluvastatin SodiumFluvastatin Sodium
0378-5121Fluvastatin Sodiumfluvastatin
0378-8020Fluvastatin Sodiumfluvastatin
0378-8021Fluvastatin Sodiumfluvastatin
0527-2580Fluvastatin SodiumFluvastatin Sodium
0781-5370FLUVASTATIN SODIUMfluvastatin sodium
0781-8017FLUVASTATIN SODIUMfluvastatin sodium
68151-1326Fluvastatin Sodiumfluvastatin
68151-1334Fluvastatin Sodiumfluvastatin
0078-0354Lescolfluvastatin sodium
68151-4471Lescolfluvastatin sodium

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.