NDC 72162-1739 – Lovastatin
Lovastatin 10 mg/1 · Tablet · Oral
Product NDC72162-1739
Product details
- Brand name
- Lovastatin
- Generic name
- Lovastatin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075991
- Marketed since
- November 25, 2002
- Listing expires
- December 31, 2026
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Lovastatin 10 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1739-0 | 1000 TABLET in 1 BOTTLE (72162-1739-0) | Aug 12, 2024 |
| 72162-1739-2 | 100 TABLET in 1 BOTTLE (72162-1739-2) | Aug 12, 2024 |
| 72162-1739-4 | 300 TABLET in 1 BOTTLE (72162-1739-4) | Aug 12, 2024 |
| 72162-1739-5 | 500 TABLET in 1 BOTTLE (72162-1739-5) | Aug 12, 2024 |
| 72162-1739-6 | 60 TABLET in 1 BOTTLE (72162-1739-6) | Aug 12, 2024 |
| 72162-1739-7 | 120 TABLET in 1 BOTTLE (72162-1739-7) | Aug 12, 2024 |
| 72162-1739-9 | 90 TABLET in 1 BOTTLE (72162-1739-9) | Aug 12, 2024 |
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