Drug recall D-0764-2026
Product
PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2453-1
Reason for recall
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
Lots and codes
Lot: P400172; Lot PA00050A, Exp 09/30/2027
Recall details
- Recalling firm
- Shilpa Medicare Limited, Jadcherla, Mahabubnagar District
- Quantity
- 18,434 10mL vials
- Distribution
- Nationwide in the USA.
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 29, 2026
Related products
- Pemrydi Rtu – drug information
- NDC 70121-2453 Pemrydi Rtu · Pemetrexed Disodium Hemipentahydrate 100 mg/10mL · Amneal Pharmaceuticals LLC
- NDC 70121-2461 Pemrydi Rtu · Pemetrexed Disodium Hemipentahydrate 500 mg/50mL · Amneal Pharmaceuticals LLC
- NDC 70121-2462 Pemrydi Rtu · Pemetrexed Disodium Hemipentahydrate 1000 mg/100mL · Amneal Pharmaceuticals LLC