FDAFDA · Food and drugs·Recall number D-0836-2020
Methylphenidate hydrochloride Extended-Release ablets USP (CII), 18 mg, 100-count bottle, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 62037-725-01
Published February 19, 2020 · Recall initiated: January 27, 2020
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
CGMP deviations: Product bottle may be absent of desiccant.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- METHYLPHENIDATE HYDROCHLORIDE
- Manufacturer
- Teva Pharmaceuticals USA
- Distributor
- USA Nationwide
- Lot
- Lot #: 1332796 A, Exp 11/2020
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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