Lovastatin
- Product NDC
- 68071-2653
- 11-digit product format
- 680712653
- Labeler code
- 68071
- Product ID
- 68071-2653_d9e29a11-c0a8-c5a0-e053-2a95a90a5831
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075551
- Marketing category
- ANDA
- Marketing start
- 2001-12-17
- Marketing end
- 0000-00-00
- Substance
- LOVASTATIN
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2653-9 | 68071265309 | 90 TABLET in 1 BOTTLE (68071-2653-9) | 90 tablet | 2022-03-10 | 0000-00-00 | No | No | Current |