Pravastatin Sodium 68180-0487
Product NDC
68180-0487- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 24, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA077917
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Pravastatin Sodium | 40 mg/1 |
Drug Class
HMG-CoA Reductase Inhibitor [EPC]Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]