Class II · Moderate risk
Ondansetron 8 mg tablet NDC 57237-0076-30 28 days supply
Lack of Processing Controls.
National Drug Code
Is NDC 57237-0076-30 recalled?
Ondansetron Hydrochloride · 30 TABLET, FILM COATED in 1 BOTTLE (57237-076-30)
Yes — this exact package was recalled
1 FDA recall names the code 57237-0076-30 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 · Oral
- Labeler
- Rising Pharma Holdings, Inc.
- Type
- Human Prescription Drug
- Product code
- 57237-0076
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
- 57237-0018 See recall 3
- 57237-0019 See recall 3
- 57237-0017 See recall 2
- 57237-0041 Penicillin V Potassium 1
- 57237-0119 See recall 1
- 57237-0221 Pioglitazone 1
Free recall alerts
Know the day your medication is recalled
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