Class I · High risk
Ceftriaxone for Injection USP
Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.
National Drug Code
Is NDC 68180-0611-01 recalled?
Ceftriaxone for Injection USP
Yes — this exact package was recalled
2 FDA recalls name the code 68180-0611-01 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.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls naming this package
Class III · Low risk
Ceftriaxone for Injection USP
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
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
- 68180-0723 Cefdinir 7
- 68180-0405 Cefixime 4
- 68180-0519 Lisinopril and Hydrochlorothiazide 4
- 68180-0422 Moxifloxacin 3
- 68180-0435 See recall 3
- 68180-0633 See recall 3
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