Class II · Moderate risk
Ondansetron HCL
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 65862-0188-30 recalled?
Ondansetron Hydrochloride · 30 TABLET, FILM COATED in 1 BOTTLE (65862-188-30)
Yes — this exact package was recalled
1 FDA recall names the code 65862-0188-30 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 8 mg/1
- Form
- Tablet, Film Coated
- Labeler
- Aurobindo Pharma Limited
- Type
- Drug for Further Processing
- Product code
- 65862-0188
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
- 65862-0053 Simvastatin 2
- 65862-0420 Sulfamethoxazole and Trimethoprim 2
- 65862-0573 Valsartan 2
- 65862-0739 Amlodipine and valsartan 2
- 65862-0840 Moxifloxacin 2
- 65862-0010 Metformin Hydrochloride 1
Free recall alerts
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