Lovastatin
- Product NDC
- 55700-244
- 11-digit product format
- 557000244
- Labeler code
- 55700
- Product ID
- 55700-244_d6d814d5-b2dd-4d9c-b5c7-36a2ebec94a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-244-90 | 55700024490 | 90 TABLET in 1 BOTTLE (55700-244-90) | 90 tablet | 2015-04-24 | 0000-00-00 | No | No | Current |