Where it's 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 |
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
68180-486-0268180-486-0368180-486-09- Official label
- DailyMed (National Library of Medicine), updated Dec 19, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?