Class II ยท Moderate risk
Pemrydi Rtu
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
National Drug Code
Is NDC 70121-2453-01 recalled?
Pemrydi Rtu · 1 VIAL in 1 CARTON (70121-2453-1) / 10 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 70121-2453-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Pemetrexed disodium
- Strength
- PEMETREXED DISODIUM HEMIPENTAHYDRATE 100 mg/10mL
- Form
- Injection · Intravenous
- Labeler
- Amneal Pharmaceuticals LLC
- Type
- Human Prescription Drug
- Product code
- 70121-2453
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 70121-1390 See recall 2
- 70121-1574 Methylprednisolone acetate 1
- 70121-1685 Exenatide 1
- 70121-1720 Magnesium Sulfate 1
- 70121-1734 Ropivacaine Hydrochloride 1
- 70121-2461 Pemrydi Rtu 1
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