Published recall report · See noticeUpdated · 1 month ago
Shilpa Medicare Limited recall: PEMRYDI RTU(pemetrexed injection), 500 mg/50 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: 70121-2461-1
PEMRYDI RTU(pemetrexed injection), 500 mg/50 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: 70121-2461-1
Current recall status is unverified. FDA does not update drug-enforcement status after publication. Check the latest official information or ask a pharmacist.
What to do
Check the lot number on your pack against this recall and follow the firm's instructions. Do not stop taking a prescribed medicine without talking to a pharmacist or doctor first.
FDA public enforcement report, opens in a new tabWhich products
PEMRYDI RTU(pemetrexed injection), 500 mg/50 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: 70121-2461-1
- Producer
- Shilpa Medicare Limited
- Brand
- PEMRYDI RTU
P400157
- Dates on pack
- Lot: P400157, Exp 08/31/2026; Lot PA00047A, Exp 09/30/2027
PA00047A
- Dates on pack
- Lot: P400157, Exp 08/31/2026; Lot PA00047A, Exp 09/30/2027
0370121246213
0370121246114
0370121245315
More detail
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
In the news
Reporting from news publishers. Follow the official notice for product advice.
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