Class III ยท Low risk
Tremfya (guselkumab)
Temperature Abuse
National Drug Code
Is NDC 57894-0640-01 recalled?
Tremfya · 1 SYRINGE in 1 CARTON (57894-640-01) / 1 mL in 1 SYRINGE
Yes — this exact package was recalled
1 FDA recall names the code 57894-0640-01 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
- Guselkumab
- Strength
- GUSELKUMAB 100 mg/mL
- Form
- Injection · Subcutaneous
- Labeler
- Janssen Biotech, Inc.
- Type
- Human Prescription Drug
- Product code
- 57894-0640
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
- 57894-0061 Stelara 1
Free recall alerts
Know the day your medication is recalled
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