Pravastatin Sodium 68462-0195
Product NDC
68462-0195- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 11, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077987
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Pravastatin Sodium | 10 mg/1 |
Drug Class
HMG-CoA Reductase Inhibitor [EPC]Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Packaging Options(2)
500 TABLET in 1 BOTTLE (68462-195-05)
90 TABLET in 1 BOTTLE (68462-195-90)