Lovastatin 68645-0566
Product NDC
68645-0566- Manufacturer
- Legacy Pharmaceutical Packaging, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2007
- Listing Expires
- December 31, 2027
- Application
- ANDA078296
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lovastatin | 20 mg/1 |
Drug Class
HMG-CoA Reductase Inhibitor [EPC]HMG-CoA Reductase Inhibitor [EPC]Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Packaging Options(1)
90 TABLET in 1 BOTTLE (68645-566-90)