Shilpa Medicare Limited recalls PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL),
See all recalls from Shilpa Medicare Limited →Recalled 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
Hazard / Issue
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot: P400172; Lot PA00050A, Exp 09/30/2027
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for PEMRYDI RTU (pemetrexed injection), →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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