NDC 16729-010 – Pravastatin Sodium
Pravastatin Sodium 40 mg/1 · Tablet · Oral
Product NDC16729-010
Product details
- Brand name
- Pravastatin Sodium
- Generic name
- Pravastatin Sodium
- Labeler
- Accord Healthcare Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207068
- Marketed since
- February 16, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Active ingredients
- Pravastatin Sodium 40 mg/1
Uses, dosage, side effects and warnings for Pravastatin Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 16729-010-15 | 90 TABLET in 1 BOTTLE (16729-010-15) | Feb 16, 2017 |
| 16729-010-16 | 500 TABLET in 1 BOTTLE (16729-010-16) | Feb 16, 2017 |
| 16729-010-17 | 1000 TABLET in 1 BOTTLE (16729-010-17) | Feb 16, 2017 |
Recalls mentioning this NDC
- D-0424-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0421-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0423-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0422-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection.
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