FDAFDA · Food and drugs·Recall number D-319-2013
Walmart Amlodipine Besylate Tablets, USP 10 mg, Rx only, 30 tablets, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge, NY. Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR. Packaged by: Legacy Pharmaceutical Packaging, LLC, Earth City, MO. NDC 68645-445-70.
Published May 22, 2013 · Recall initiated: April 22, 2013
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
Labeling: Label Error on Declared Strength-The recalled product has a misprint on the Amoldipine 10 mg label, 5 mg is listed in the USP description. Tablet strength is 10 mg.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Legacy Pharmaceutical Packaging LLC
- Distributor
- Nationwide
- Lot
- Lot # 130251, 130252, 130253 Exp date: 11/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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