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 ID | 0527-2580_c1be7832-b98b-d8fb-e053-2995a90a9b83 |
| NDC | 0527-2580 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Fluvastatin Sodium |
| Generic Name | Fluvastatin Sodium |
| Dosage Form | Tablet, Film Coated, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-05-07 |
| Marketing Category | ANDA / |
| Application Number | ANDA209397 |
| Labeler Name | Lannett Company, Inc. |
| Substance Name | FLUVASTATIN SODIUM |
| Active Ingredient Strength | 80 mg/1 |
| Pharm Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |