NDC 68001-316 – Lovastatin
Lovastatin 40 mg/1 · Tablet · Oral
Product NDC68001-316
Product details
- Brand name
- Lovastatin
- Generic name
- Lovastatin
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078296
- Marketed since
- November 1, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Lovastatin 40 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68001-316-00 | 100 TABLET in 1 BOTTLE (68001-316-00) | Feb 7, 2017 |
| 68001-316-08 | 1000 TABLET in 1 BOTTLE (68001-316-08) | Feb 7, 2017 |
Recalls mentioning this NDC
- D-1584-2019 Aug 14, 2019 · Class III
CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
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