0527-2580 : Fluvastatin Sodium 80 mg Oral Tablet, Film Coated, Extended Release


NDC: 0527-2580
Labeler: Lannett Company, Inc.
Product Type: Human Prescription Drug
Drug Name:  Fluvastatin Sodium
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA209397
Rev. Date: 


NDC Package Codes:

  • 0527-2580-32: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (0527‑2580‑32)
  • 0527-2580-37: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (0527‑2580‑37)

Active Ingredients:

  • Fluvastatin Sodium

Dosage Strength:

  • 80 mg

Pharmaceutical Classes:

  • HMG-CoA Reductase Inhibitor [EPC]
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 0093-7446 Fluvastatin Sodium 80 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0378-5121 Fluvastatin Sodium 80 mg Oral Tablet, Film Coated, Extended Release by Mylan Pharmaceuticals Inc.
  • 0378-8020 Fluvastatin (As Fluvastatin Sodium) 20 mg Oral Capsule by Mylan Pharmaceuticals Inc.
  • 0378-8021 Fluvastatin (As Fluvastatin Sodium) 40 mg Oral Capsule by Mylan Pharmaceuticals Inc.
  • 0781-5370 Fluvastatin 80 mg 24 Hr Extended Release Tablet by Sandoz Inc
  • 68151-1326 Fluvastatin Sodium 20 mg Oral Capsule by Carilion Materials Management
  • 68151-1334 Fluvastatin Sodium 40 mg Oral Capsule by Carilion Materials Management

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.