Lovastatin
- Product NDC
- 68788-2634
- 11-digit product format
- 687882634
- Labeler code
- 68788
- Product ID
- 68788-2634_d17256be-9775-49d0-aecc-3ee197ecaa17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA075828
- Marketing category
- ANDA
- Marketing start
- 2013-03-18
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record