Class II · Moderate risk
Ondansetron Injection
Failed pH Specifications
National Drug Code
Is NDC 36000-0012-25 recalled?
Ondansetron Hydrochloride · 25 VIAL, SINGLE-DOSE in 1 CARTON (36000-012-25) / 2 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 36000-0012-25 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
- Ondansetron Hydrochloride
- Strength
- ONDANSETRON HYDROCHLORIDE 2 mg/mL
- Form
- Solution · Intramuscular, Intravenous
- Labeler
- Baxter Healthcare Corporation
- Type
- Human Prescription Drug
- Product code
- 36000-0012
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
- 36000-0002 See recall 3
- 36000-0048 See recall 3
- 36000-0003 See recall 2
- 36000-0046 See recall 2
- 36000-0047 See recall 2
- 36000-0306 Acetaminophen 2
Free recall alerts
Know the day your medication is recalled
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