Class II ยท Moderate risk
Aloprim (allopurinol sodium)
Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.
National Drug Code
Is NDC 67457-0187-50 recalled?
Aloprim · 1 VIAL, GLASS in 1 CARTON (67457-187-50) / 25 mL in 1 VIAL, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 67457-0187-50 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.
- Active ingredient
- Allopurinol
- Strength
- ALLOPURINOL SODIUM 500 mg/25mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Mylan Institutional LLC
- Type
- Human Prescription Drug
- Product code
- 67457-0187
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
- 67457-0153 Amiodarone Hydrochloride 2
- 67457-0386 Mycophenolate Mofetil 2
- 67457-0445 Rifampin 2
- 67457-0196 Thiamine Hydrochloride 1
- 67457-0197 Tranexamic Acid 1
- 67457-0218 Duraclon 1
Free recall alerts
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