Lovastatin
- Product NDC
- 68071-4271
- 11-digit product format
- 680714271
- Labeler code
- 68071
- Product ID
- 68071-4271_e767aa2c-50dc-bf30-e053-2995a90a4a4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2023-12-31
- 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 |
|---|
| 68071-4271-3 | 68071427103 | 30 TABLET in 1 BOTTLE (68071-4271-3) | 30 tablet | 2018-02-06 | 0000-00-00 | No | No | Current |
| 68071-4271-6 | 68071427106 | 60 TABLET in 1 BOTTLE (68071-4271-6) | 60 tablet | 2018-02-06 | 0000-00-00 | No | No | Current |
| 68071-4271-9 | 68071427109 | 90 TABLET in 1 BOTTLE (68071-4271-9) | 90 tablet | 2018-02-06 | 0000-00-00 | No | No | Current |