Lovastatin
- Product NDC
- 50436-6500
- 11-digit product format
- 504366500
- Labeler code
- 50436
- Product ID
- 50436-6500_ad3afc5a-6d08-4888-8f27-98450a14b2d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record