FDAFDA · Food and drugs·Recall number D-0092-2018
Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, NDC 68180-487-09
Published November 29, 2017 · Recall initiated: November 17, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PRAVASTATIN SODIUM
- Manufacturer
- Lupin Limited
- Distributor
- Product was distributed throughout the United States, including Puerto Rico.
- UPC
- 0368180487098
- Lot
- Lot # G702459, Exp 2/20
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- India
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