Class II ยท Moderate risk
Imitrex STATdose System
Lack of Assurance of Sterility: A small number of pre-filled syringes may contain needles which protrude through the needle shield.
National Drug Code
Is NDC 0173-0479-00 recalled?
Imitrex · 2 SYRINGE in 1 PACKAGE (0173-0479-00) / .5 mL in 1 SYRINGE
Yes — this exact package was recalled
1 FDA recall names the code 0173-0479-00 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
- sumatriptan
- Strength
- SUMATRIPTAN SUCCINATE 6 mg/.5mL
- Form
- Injection · Subcutaneous
- Labeler
- GlaxoSmithKline LLC
- Type
- Human Prescription Drug
- Product code
- 0173-0479
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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