LOVASTATIN
- Product NDC
- 54458-916
- 11-digit product format
- 544580916
- Labeler code
- 54458
- Product ID
- 54458-916_7e62b171-b224-4ffd-a785-f57ee81abeac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOVASTATIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- International Laboratories, LLC
- Application
- ANDA075551
- Marketing category
- ANDA
- Marketing start
- 2008-03-27
- Marketing end
- 0000-00-00
- Substance
- LOVASTATIN
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record