Class II ยท Moderate risk
Prasugrel HCI
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
National Drug Code
Is NDC 51407-0445-30 recalled?
Prasugrel · 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-445-30)
Yes — this exact package was recalled
1 FDA recall names the code 51407-0445-30 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.
1 of these recalls is still ongoing.
- Active ingredient
- Prasugrel
- Strength
- PRASUGREL HYDROCHLORIDE 10 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Golden State Medical Supply, Inc.
- Type
- Human Prescription Drug
- Product code
- 51407-0445
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
- 51407-0268 Niacin 2
- 51407-0097 See recall 1
- 51407-0098 See recall 1
- 51407-0129 See recall 1
- 51407-0192 Ezetimibe and Simvastatin 1
- 51407-0193 Ezetimibe and Simvastatin 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.