Class II ยท Moderate risk
PAROXETINE tablets
Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine
National Drug Code
Is NDC 60429-0737-90 recalled?
Paroxetine · 90 TABLET, FILM COATED in 1 BOTTLE (60429-737-90)
Yes — this exact package was recalled
1 FDA recall names the code 60429-0737-90 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
- paroxetine hydrochloride
- Strength
- PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Golden State Medical Supply, Inc.
- Type
- Human Prescription Drug
- Product code
- 60429-0737
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
- 60429-0316 See recall 4
- 60429-0317 See recall 4
- 60429-0318 See recall 3
- 60429-0640 See recall 2
- 60429-0641 See recall 2
- 60429-0642 See recall 2
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.