Class II ยท Moderate risk
Paroxetine Hydrochloride Tablets USP
Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
National Drug Code
Is NDC 60505-0084-01 recalled?
Paroxetine · 30 TABLET, FILM COATED in 1 BOTTLE (60505-0084-1)
Yes — this exact package was recalled
1 FDA recall names the code 60505-0084-01 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
- paroxetine hydrochloride
- Strength
- PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Apotex Corp.
- Type
- Human Prescription Drug
- Product code
- 60505-0084
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
Know the day your medication is recalled
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