Class II · Moderate risk
Tramadol Hydrochloride Tablets USP 100mg
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 52817-0196-10 recalled?
Tramadol Hydrochloride · 100 TABLET, COATED in 1 BOTTLE (52817-196-10)
Yes — this exact package was recalled
1 FDA recall names the code 52817-0196-10 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
- Tramadol Hydrochloride
- Strength
- TRAMADOL HYDROCHLORIDE 100 mg/1
- Form
- Tablet, Coated · Oral
- Labeler
- Trupharma LLC
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 52817-0196
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
- 52817-0360 Metoprolol Tartrate 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.