NDC 75834-256 – Atorvastatin calcium
Atorvastatin 20 mg/1 · Tablet · Oral
Product NDC75834-256
Product details
- Brand name
- Atorvastatin calcium
- Generic name
- Atorvastatin calcium
- Labeler
- NIVAGEN PHARMACEUTICALS, INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA213853
- Marketed since
- August 26, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Atorvastatin 20 mg/1
Uses, dosage, side effects and warnings for Atorvastatin Calcium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 75834-256-01 | 1000 TABLET in 1 BOTTLE (75834-256-01) | Aug 26, 2020 |
| 75834-256-05 | 5000 TABLET in 1 BOTTLE (75834-256-05) | Aug 26, 2020 |
| 75834-256-50 | 500 TABLET in 1 BOTTLE (75834-256-50) | Aug 26, 2020 |
| 75834-256-90 | 90 TABLET in 1 BOTTLE (75834-256-90) | Aug 26, 2020 |
Recalls mentioning this NDC
- D-0001-2025 Oct 9, 2024 · Class II
Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400 mg tablet was found in a 1000-count bottle of Atorvastatin Calcium Tablets, USP 40 mg.
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