NDC 0093-7201 – Pravastatin Sodium
Pravastatin Sodium 20 mg/1 · Tablet · Oral
Product NDC0093-7201
Product details
- Brand name
- Pravastatin Sodium
- Generic name
- Pravastatin Sodium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076056
- Marketed since
- April 25, 2006
- Marketing end
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-7201-10 | 1000 TABLET in 1 BOTTLE (0093-7201-10) | Apr 25, 2006 |
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