Lovastatin
- Product NDC
- 63629-6436
- 11-digit product format
- 636296436
- Labeler code
- 63629
- Product ID
- 63629-6436_f1e318bb-3039-4bbb-9481-b53e329ce63f
- 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
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 63629-6436-1 | 63629643601 | 30 TABLET in 1 BOTTLE (63629-6436-1) | 30 tablet | 2016-02-03 | 0000-00-00 | No | No | Current |
| 63629-6436-2 | 63629643602 | 90 TABLET in 1 BOTTLE (63629-6436-2) | 90 tablet | 2015-11-03 | 0000-00-00 | No | No | Current |