NDC 16714-559 – Pravastatin Sodium
Pravastatin Sodium 20 mg/1 · Tablet · Oral
Product NDC16714-559
Product details
- Brand name
- Pravastatin Sodium
- Generic name
- Pravastatin Sodium
- Labeler
- NorthStar RxLLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077987
- Marketed since
- August 12, 2022
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 16714-559-01 | 90 TABLET in 1 BOTTLE (16714-559-01) | Aug 12, 2022 |
| 16714-559-02 | 500 TABLET in 1 BOTTLE (16714-559-02) | Aug 12, 2022 |
Recalls mentioning this NDC
- D-0350-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-0349-2025 Apr 16, 2025 · Class II
CGMP Deviations
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