Pravastatin Sodium 61919-0708
Product NDC
61919-0708- Manufacturer
- Direct_rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 15, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA207068
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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]
Packaging Options(1)
30 TABLET in 1 BOTTLE (61919-708-30)