NDC 71335-9642 – Simvastatin
Simvastatin 20 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-9642
Product details
- Brand name
- Simvastatin
- Generic name
- Simvastatin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078103
- Marketed since
- June 14, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Simvastatin 20 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9642-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-9642-1) | Feb 27, 2023 |
| 71335-9642-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-9642-2) | Feb 27, 2023 |
| 71335-9642-3 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-9642-3) | Mar 3, 2025 |
| 71335-9642-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-9642-4) | Feb 17, 2023 |
| 71335-9642-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-9642-5) | Mar 12, 2025 |
| 71335-9642-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-9642-6) | Apr 15, 2026 |
| 71335-9642-7 | 3 TABLET, FILM COATED in 1 BOTTLE (71335-9642-7) | Apr 15, 2026 |
| 71335-9642-8 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-9642-8) | Apr 15, 2026 |
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