NDC 55111-230 – Pravastatin sodium
Pravastatin Sodium 20 mg/1 · Tablet · Oral
Product NDC55111-230
Product details
- Brand name
- Pravastatin sodium
- Generic name
- Pravastatin sodium
- Labeler
- Dr.Reddy's Laboratories Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076714
- Marketed since
- December 31, 2009
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 55111-230-01 | 100 TABLET in 1 BOTTLE (55111-230-01) | Dec 31, 2009 |
| 55111-230-05 | 500 TABLET in 1 BOTTLE (55111-230-05) | Dec 31, 2009 |
| 55111-230-30 | 30 TABLET in 1 BOTTLE (55111-230-30) | Dec 31, 2009 |
| 55111-230-90 | 90 TABLET in 1 BOTTLE (55111-230-90) | Dec 31, 2009 |
Recalls mentioning this NDC
- D-1038-2017 Aug 9, 2017 · Class III
Failed Impurities/Degradation Specifications: high out of specification results for related impurity for lot C700220.
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