Lovastatin
- Product NDC
- 68071-3615
- 11-digit product format
- 680713615
- Labeler code
- 68071
- Product ID
- 68071-3615_1b30c378-b8d4-9650-e063-6394a90ae8f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078296
- Marketing category
- ANDA
- Marketing start
- 2007-11-01
- Substance
- LOVASTATIN
- Active strength
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9LHU78OQFD | LOVASTATIN | 75330-75-5 | LOVASTATIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3615-1 | 68071361501 | 100 TABLET in 1 BOTTLE (68071-3615-1) | 100 tablet | 2024-05-30 | No | No | Historical |