Class II ยท Moderate risk
Sertraline Hydrochloride Tablets USP
Defective container - seal not adhering to bottles
National Drug Code
Is NDC 68180-0353-09 recalled?
Sertraline Hydrochloride · 90 TABLET, FILM COATED in 1 BOTTLE (68180-353-09)
Yes — this exact package was recalled
1 FDA recall names the code 68180-0353-09 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
- Sertraline Hydrochloride
- Strength
- SERTRALINE HYDROCHLORIDE 100 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Lupin Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 68180-0353
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
- 68180-0723 Cefdinir 7
- 68180-0405 Cefixime 4
- 68180-0519 Lisinopril and Hydrochlorothiazide 4
- 68180-0422 Moxifloxacin 3
- 68180-0435 See recall 3
- 68180-0633 See recall 3
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.