Class III ยท Low risk
Allopurinol Tablets
Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
National Drug Code
Is NDC 0603-2116-28 recalled?
Allopurinol · 500 TABLET in 1 BOTTLE, PLASTIC (0603-2116-28)
Yes — this exact package was recalled
1 FDA recall names the code 0603-2116-28 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 300 mg/1
- Form
- Tablet · Oral
- Labeler
- Par Health USA, LLC
- Type
- Human Prescription Drug
- Product code
- 0603-2116
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
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