Lovastatin
- Product NDC
- 71205-992
- 11-digit product format
- 712050992
- Labeler code
- 71205
- Product ID
- 71205-992_e637904d-8af6-47fe-b10e-db813d5531bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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 |
|---|
| 71205-992-00 | 71205099200 | 100 TABLET in 1 BOTTLE (71205-992-00) | 100 tablet | 2020-04-01 | No | No | Historical |
| 71205-992-11 | 71205099211 | 1000 TABLET in 1 BOTTLE (71205-992-11) | 1000 tablet | 2020-04-01 | No | No | Historical |
| 71205-992-30 | 71205099230 | 30 TABLET in 1 BOTTLE (71205-992-30) | 30 tablet | 2020-04-01 | No | No | Historical |
| 71205-992-55 | 71205099255 | 500 TABLET in 1 BOTTLE (71205-992-55) | 500 tablet | 2020-04-01 | No | No | Historical |
| 71205-992-60 | 71205099260 | 60 TABLET in 1 BOTTLE (71205-992-60) | 60 tablet | 2020-04-01 | No | No | Historical |
| 71205-992-90 | 71205099290 | 90 TABLET in 1 BOTTLE (71205-992-90) | 90 tablet | 2020-04-01 | No | No | Historical |