Lovastatin
- Product NDC
- 63629-1019
- 11-digit product format
- 636291019
- Labeler code
- 63629
- Product ID
- 63629-1019_c18af9e7-b364-4f53-bd54-13b15797c7b5
- 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
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1019-0 | 63629101900 | 1000 TABLET in 1 BOTTLE (63629-1019-0) | 1000 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |
| 63629-1019-1 | 63629101901 | 100 TABLET in 1 BOTTLE (63629-1019-1) | 100 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |
| 63629-1019-2 | 63629101902 | 30 TABLET in 1 BOTTLE (63629-1019-2) | 30 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |
| 63629-1019-3 | 63629101903 | 300 TABLET in 1 BOTTLE (63629-1019-3) | 300 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |
| 63629-1019-5 | 63629101905 | 500 TABLET in 1 BOTTLE (63629-1019-5) | 500 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |
| 63629-1019-6 | 63629101906 | 60 TABLET in 1 BOTTLE (63629-1019-6) | 60 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |
| 63629-1019-8 | 63629101908 | 800 TABLET in 1 BOTTLE (63629-1019-8) | 800 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |