NDC 68180-468 – Lovastatin
Lovastatin 20 mg/1 · Tablet · Oral
Product NDC68180-468
Product details
- Brand name
- Lovastatin
- Generic name
- Lovastatin
- Labeler
- Lupin Pharmaceuticals, Inc.
- 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 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68180-468-01 | 100 TABLET in 1 BOTTLE (68180-468-01) | Nov 1, 2007 |
| 68180-468-03 | 1000 TABLET in 1 BOTTLE (68180-468-03) | Nov 1, 2007 |
| 68180-468-05 | 5000 TABLET in 1 BOTTLE (68180-468-05) | Nov 1, 2007 |
| 68180-468-07 | 60 TABLET in 1 BOTTLE (68180-468-07) | Nov 1, 2007 |
Recalls mentioning this NDC
- D-0513-2019 Feb 27, 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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