Lovastatin
- Product NDC
- 63629-1191
- 11-digit product format
- 636291191
- Labeler code
- 63629
- Product ID
- 63629-1191_4418be45-ac95-468d-8603-53d72198b4b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075991
- Marketing category
- ANDA
- Marketing start
- 2002-11-25
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9LHU78OQFD | LOVASTATIN | 75330-75-5 | LOVASTATIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-1191-1 | 63629119101 | 1000 TABLET in 1 BOTTLE (63629-1191-1) | 1000 tablet | 2002-11-25 | No | No | Historical |