Drug recall D-0943-2017
Product
Amitriptyline HCl Tablets, USP 25 mg, Packaged in a)100-count bottles (NDC 0781-1487-01) and b) 1000-count bottles ( NDC 0781-1487-10), Rx only, Manufactured by Sandoz Inc., Princeton, NJ 08540
Reason for recall
Cross Contamination With Other Product: Imipramine
Lots and codes
Lot #: a) GR3831, GS9690, Exp. 08/2019; b) GR3832, Exp. 08/2019.
Recall details
- Recalling firm
- Sandoz Incorporated, Broomfield, CO
- Quantity
- 38,234 bottles
- Distribution
- Product was distributed throughout the United States
- Type
- Voluntary: Firm initiated
- Recall initiated
- June 16, 2017
- Terminated
- January 14, 2019
Related products
- Amitriptyline Hydrochloride – drug information
- NDC 0781-1491 Amitriptyline Hydrochloride · Amitriptyline Hydrochloride 150 mg/1 · Sandoz Inc
- NDC 0781-1486 Amitriptyline Hydrochloride · Amitriptyline Hydrochloride 10 mg/1 · Sandoz Inc
- NDC 0781-1489 Amitriptyline Hydrochloride · Amitriptyline Hydrochloride 75 mg/1 · Sandoz Inc
- NDC 0781-1488 Amitriptyline Hydrochloride · Amitriptyline Hydrochloride 50 mg/1 · Sandoz Inc
- NDC 0781-1490 Amitriptyline Hydrochloride · Amitriptyline Hydrochloride 100 mg/1 · Sandoz Inc
- NDC 0781-1487 Amitriptyline Hydrochloride · Amitriptyline Hydrochloride 25 mg/1 · Sandoz Inc