Class II ยท Moderate risk
Guanfacine Extended-Release Tablets 2 mg
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
National Drug Code
Is NDC 60505-3928-01 recalled?
Guanfacine extended-release · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-3928-1)
Yes — this exact package was recalled
1 FDA recall names the code 60505-3928-01 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
- guanfacine
- Strength
- GUANFACINE HYDROCHLORIDE 2 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Apotex Corp.
- Type
- Human Prescription Drug
- Product code
- 60505-3928
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
- 60505-0589 Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 3
- 60505-0829 Fluticasone Propionate 3
- 60505-2580 Atorvastatin Calcium 3
- 60505-0595 See recall 2
- 60505-0596 See recall 2
- 60505-0773 See recall 2
Free recall alerts
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