Class II ยท Moderate risk
Clonidine Transdermal System
Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.
National Drug Code
Is NDC 51862-0455-04 recalled?
Clonidine
Yes — this exact package was recalled
1 FDA recall names the code 51862-0455-04 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
- Clonidine
- Strength
- CLONIDINE .3 mg/24h
- Form
- Patch, Extended Release · Transdermal
- Labeler
- Mayne Pharma Inc.
- Type
- Human Prescription Drug
- Product code
- 51862-0455
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
- 51862-0146 See recall 1
- 51862-0159 See recall 1
- 51862-0185 See recall 1
- 51862-0186 See recall 1
- 51862-0295 Fabior 1
- 51862-0604 See recall 1
Free recall alerts
Know the day your medication is recalled
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