Class II · Moderate risk
Clonidine Transdermal System
CGMP Deviations: use of an unapproved raw material
National Drug Code
Is NDC 0591-3510-04 recalled?
Clonidine transdermal system · 4 POUCH in 1 CARTON (0591-3510-04) / 1 PATCH in 1 POUCH (0591-3510-54) / 7 d in 1 PATCH
Yes — this exact package was recalled
1 FDA recall names the code 0591-3510-04 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.
1 of these recalls is still ongoing.
- Active ingredient
- Clonidine
- Strength
- CLONIDINE .3 mg/d
- Form
- Patch · Transdermal
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug
- Product code
- 0591-3510
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
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