NDC 68180-486 – Pravastatin Sodium
Pravastatin Sodium 20 mg/1 · Tablet · Oral
Product NDC68180-486
Product details
- Brand name
- Pravastatin Sodium
- Generic name
- Pravastatin Sodium
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077917
- Marketed since
- July 24, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Pravastatin Sodium 20 mg/1
Uses, dosage, side effects and warnings for Pravastatin Sodium →
Package NDC codes (0)
| Package NDC | Description | Since |
|---|
Recalls mentioning this NDC
- D-0092-2018 Nov 29, 2017 · Class II
Presence of foreign tablets/capsules: This product lot is being recalled due to a pharmacy complaint where one Duloxetine Delayed Release Capsule, 30mg was found in a Pravastatin Sodium Tablets USP,…
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