Fluvastatin 00093-7442
Product NDC
00093-7442- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 5, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA078407
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluvastatin Sodium | 20 mg/1 |
Drug Class
HMG-CoA Reductase Inhibitor [EPC]Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Packaging Options(2)
100 CAPSULE in 1 BOTTLE (0093-7442-01)
30 CAPSULE in 1 BOTTLE (0093-7442-56)