NDC 71335-0819 – Lovastatin
Lovastatin 20 mg/1 · Tablet · Oral
Product NDC71335-0819
Product details
- Brand name
- Lovastatin
- Generic name
- Lovastatin
- Labeler
- Bryant Ranch Prepack
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0819-1 | 30 TABLET in 1 BOTTLE (71335-0819-1) | May 8, 2018 |
| 71335-0819-2 | 100 TABLET in 1 BOTTLE (71335-0819-2) | Apr 4, 2024 |
| 71335-0819-3 | 60 TABLET in 1 BOTTLE (71335-0819-3) | Apr 4, 2024 |
| 71335-0819-4 | 90 TABLET in 1 BOTTLE (71335-0819-4) | Jun 22, 2018 |
| 71335-0819-5 | 20 TABLET in 1 BOTTLE (71335-0819-5) | Apr 4, 2024 |
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