Pravastatin Sodium 00904-5892
Product NDC
00904-5892- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 18, 2011
- Listing Expires
- December 31, 2027
- Application
- ANDA076341
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Pravastatin Sodium | 20 mg/1 |
Drug Class
HMG-CoA Reductase Inhibitor [EPC]Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Packaging Options(1)
100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5892-61) / 1 TABLET in 1 BLISTER PACK