Drug recall D-0498-2024
Product
Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA, NDC 33342-050-44
Reason for recall
Presence of foreign substance: plastic-like substance.
Lots and codes
Lot #: BLK2304A, Exp. 07/31/2025
Recall details
- Recalling firm
- MACLEODS PHARMA USA, INC, Princeton, NJ
- Quantity
- 1,048 bottles
- Distribution
- USA Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 7, 2024
Related products
- Losartan Potassium and Hydrochlorothiazide – drug information
- NDC 33342-051 Losartan potassium and Hydrochlorothiazide · Losartan Potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1 · Macleods Pharmaceuticals Limited
- NDC 33342-050 Losartan potassium and Hydrochlorothiazide · Losartan Potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 · Macleods Pharmaceuticals Limited
- NDC 33342-052 Losartan potassium and Hydrochlorothiazide · Losartan Potassium 100 mg/1; Hydrochlorothiazide 25 mg/1 · Macleods Pharmaceuticals Limited