NDC 54458-927
Pravastatin Sodium 10 mg tablet
On the label: International Laboratories, LLC. It's repackaged: International Laboratories, LLC rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-0771.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- International Laboratories, LLC, Seminole, Florida, United States · repackages it and relabels it
Recalls
- Jan 12, 2018 · Class II · International Laboratories, Inc.
Presence of Foreign Tablets/Capsules: bottles could contain both pravastatin sodium 10 mg and 20 mg tablets in the same bottle.
Lots: Lot: 117093A, Exp. 06/19
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
- Strength
- 10 mg
- Approval
- ANDA ANDA076056
- On the market since
- Apr 26, 2013
- Package NDCs
54458-927-1054458-927-1254458-927-16- Official label
- DailyMed (National Library of Medicine), updated Mar 29, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?