Lovastatin
- Product NDC
- 63629-6346
- 11-digit product format
- 636296346
- Labeler code
- 63629
- Product ID
- 63629-6346_8c49858d-c873-4737-98d9-8b1523d8de60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078296
- Marketing category
- ANDA
- Marketing start
- 2007-11-01
- 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
- 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 |
|---|
| 63629-6346-1 | 63629634601 | 30 TABLET in 1 BOTTLE (63629-6346-1) | 30 tablet | 2015-09-17 | 0000-00-00 | No | No | Current |
| 63629-6346-2 | 63629634602 | 90 TABLET in 1 BOTTLE (63629-6346-2) | 90 tablet | 2015-10-15 | 0000-00-00 | No | No | Current |