Drug recall D-0175-2024
Product
Dicyclomine Hydrochloride Tablets, USP 20 mg, 100 Tablets, Rx only, Manufactured For: Teva Pharmaceuticals USA, Parsippany, NJ 07054. NDC: 0591-0795-01
Reason for recall
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots and codes
Batch 3197790
Recall details
- Recalling firm
- CARDINAL HEALTHCARE, Dublin, OH
- Quantity
- 1 unit
- Distribution
- Nationwide USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 26, 2022
- Terminated
- September 29, 2024
Related products
- Dicyclomine Hydrochloride – drug information
- NDC 0591-0794 Dicyclomine Hydrochloride · Dicyclomine Hydrochloride 10 mg/1 · Actavis Pharma, Inc.
- NDC 0591-0795 Dicyclomine Hydrochloride · Dicyclomine Hydrochloride 20 mg/1 · Actavis Pharma, Inc.