LOVASTATIN
- Product NDC
- 61919-290
- 11-digit product format
- 619190290
- Labeler code
- 61919
- Product ID
- 61919-290_67622404-7018-4235-e053-2a91aa0a0b3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOVASTATIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA075991
- Marketing category
- ANDA
- Marketing start
- 2018-03-14
- 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