LOVASTATIN
- Product NDC
- 54458-937
- 11-digit product format
- 544580937
- Labeler code
- 54458
- Product ID
- 54458-937_409cb06e-21c2-4462-b1e8-480e30882c05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOVASTATIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- International Laboratories, LLC
- Application
- ANDA078296
- Marketing category
- ANDA
- Marketing start
- 2010-04-03
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
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 |
|---|
| 54458-937-10 | 54458093710 | 30 TABLET in 1 BLISTER PACK (54458-937-10) | 30 tablet | 2010-04-03 | 0000-00-00 | No | No | Current |
| 54458-937-16 | 54458093716 | 30 TABLET in 1 BOTTLE (54458-937-16) | 30 tablet | 2017-04-05 | 0000-00-00 | No | No | Current |