Class II ยท Moderate risk
Pioglitazone Tablets USP
Superpotent and Failed Tablet/Capsule Specifications
National Drug Code
Is NDC 57237-0221-05 recalled?
Pioglitazone · 500 TABLET in 1 BOTTLE (57237-221-05)
Yes — this exact package was recalled
1 FDA recall names the code 57237-0221-05 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
- Pioglitazone
- Strength
- PIOGLITAZONE HYDROCHLORIDE 45 mg/1
- Form
- Tablet · Oral
- Labeler
- Rising Pharma Holdings, Inc.
- Type
- Human Prescription Drug
- Product code
- 57237-0221
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
- 57237-0076 Ondansetron Hydrochloride 1
- 57237-0119 See recall 1
Free recall alerts
Know the day your medication is recalled
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