Class II · Moderate risk
Trazodone Hydrochloride Tablets
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 0904-6868-61 recalled?
Trazodone Hydrochloride · 100 BLISTER PACK in 1 CARTON (0904-6868-61) / 1 TABLET in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0904-6868-61 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
- Trazodone Hydrochloride
- Strength
- TRAZODONE HYDROCHLORIDE 50 mg/1
- Form
- Tablet · Oral
- Labeler
- Major Pharmaceuticals
- Type
- Human Prescription Drug
- Product code
- 0904-6868
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
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.