NDC 0093-7442 – Fluvastatin
Fluvastatin Sodium 20 mg/1 · Capsule · Oral
Product NDC0093-7442
Product details
- Brand name
- Fluvastatin
- Generic name
- Fluvastatin
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078407
- Marketed since
- July 5, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Fluvastatin Sodium 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0093-7442-01 | 100 CAPSULE in 1 BOTTLE (0093-7442-01) | Jul 12, 2012 |
| 0093-7442-56 | 30 CAPSULE in 1 BOTTLE (0093-7442-56) | Jul 5, 2012 |
Recalls mentioning this NDC
- D-1430-2014 Jul 16, 2014 · Class II
Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, Inc. is voluntarily recalling one lot of Fluvastatin Capsules USP, 20 mg due to a customer complaint trend regarding capsule breakage.
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