Class II ยท Moderate risk
Allopurinol Tablets USP
Presence of Foreign Substance: Presence of a small piece of green plastic embedded in the crack towards the edge of the tablet.
National Drug Code
Is NDC 16729-0134-01 recalled?
Allopurinol · 100 TABLET in 1 BOTTLE (16729-134-01)
Yes — this exact package was recalled
1 FDA recall names the code 16729-0134-01 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.
- Active ingredient
- allopurinol
- Strength
- ALLOPURINOL 100 mg/1
- Form
- Tablet · Oral
- Labeler
- Accord Healthcare Inc.
- Type
- Human Prescription Drug
- Product code
- 16729-0134
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
- 16729-0447 Levothyroxine sodium 4
- 16729-0448 Levothyroxine sodium 3
- 16729-0450 Levothyroxine sodium 3
- 16729-0452 Levothyroxine sodium 3
- 16729-0182 Hydrochlorothiazide 2
- 16729-0434 Daptomycin 2
Free recall alerts
Know the day your medication is recalled
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