NDC 71335-0947
Pravastatin Sodium 20 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-486.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- Nov 17, 2017 · Class II · Lupin Limited
Presence of foreign tablets/capsules: This product lot is being recalled due to a pharmacy complaint where one Duloxetine Delayed Release Capsule, 30mg was found in a Pravastatin Sodium Tablets USP, 40mg bottle.
Lots: Lot # G702459, Exp 2/20
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Pravastatin: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA077917
- On the market since
- Jul 24, 2008
- Package NDCs
71335-0947-171335-0947-271335-0947-371335-0947-471335-0947-5- Official label
- DailyMed (National Library of Medicine), updated Apr 4, 2024
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