NDC 35356-919 – Pravastatin Sodium
Pravastatin Sodium 20 mg/1 · Tablet · Oral
Product NDC35356-919
Product details
- Brand name
- Pravastatin Sodium
- Generic name
- Pravastatin sodium
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076341
- Marketed since
- July 18, 2011
- Marketing end
- April 30, 2028
- 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 |
|---|---|---|
| 35356-919-30 | 30 TABLET in 1 BOTTLE (35356-919-30) | Jul 18, 2011 |
| 35356-919-90 | 90 TABLET in 1 BOTTLE (35356-919-90) | Jul 18, 2011 |
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