Lovastatin
- Product NDC
- 0185-0070
- 11-digit product format
- 001850070
- Labeler code
- 0185
- Product ID
- 0185-0070_10abce48-8002-4ae6-acaf-ddccf3f7e2a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA075636
- Marketing category
- ANDA
- Marketing start
- 2001-12-17
- Marketing end
- 2021-05-31
- Substance
- LOVASTATIN
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0185-0070-01 | 00185007001 | 100 TABLET in 1 BOTTLE (0185-0070-01) | 100 tablet | 2001-12-17 | 2021-05-31 | No | No | Current |
| 0185-0070-10 | 00185007010 | 1000 TABLET in 1 BOTTLE (0185-0070-10) | 1000 tablet | 2001-12-17 | 2021-05-31 | No | No | Current |
| 0185-0070-60 | 00185007060 | 60 TABLET in 1 BOTTLE (0185-0070-60) | 60 tablet | 2001-12-17 | 2021-05-31 | No | No | Current |