Lovastatin
- Product NDC
- 0440-6694
- 11-digit product format
- 004406694
- Labeler code
- 0440
- Product ID
- 0440-6694_c8e4181e-e204-4582-9e24-29633bde5f2b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Liberty Pharmaceuticals, Inc.
- Application
- ANDA075991
- Marketing category
- ANDA
- Marketing start
- 2002-11-25
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record