NDC 0093-7446 – Fluvastatin Sodium
Fluvastatin Sodium 80 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0093-7446
Product details
- Brand name
- Fluvastatin Sodium
- Generic name
- Fluvastatin Sodium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079011
- Marketed since
- June 2, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Fluvastatin Sodium 80 mg/1
Uses, dosage, side effects and warnings for Fluvastatin Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0093-7446-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-01) | Jun 2, 2016 |
| 0093-7446-56 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-56) | Jun 2, 2016 |
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- 0527-2580 Fluvastatin Sodium 80 mg/1 · Tablet, Film Coated, Extended Release · Lannett Company, Inc.
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- 0378-8021 Fluvastatin Sodium 40 mg/1 · Capsule · Mylan Pharmaceuticals Inc.
- 0781-8017 Fluvastatin Sodium 80 mg/1 · Tablet, Extended Release · Sandoz Inc