Class II ยท Moderate risk
OXcarbazepine Tablet
Labeling:Label Mixup; OXcarbazepine Tablet, 150 mg may be potentially mislabeled as traZODone HCl, Tablet, 50 mg, NDC 50111043301, Pedigree: AD54562_1, EXP: 5/20/2014.
National Drug Code
Is NDC 62756-0183-88 recalled?
Oxcarbazepine
Yes — this exact package was recalled
1 FDA recall names the code 62756-0183-88 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
- Oxcarbazepine
- Strength
- OXCARBAZEPINE 150 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 62756-0183
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
- 62756-0015 Testosterone Cypionate 7
- 62756-0142 Metformin Hydrochloride 4
- 62756-0016 Testosterone Cypionate 2
- 62756-0185 Oxcarbazepine 2
- 62756-0233 Amphotericin B 2
- 62756-0522 sumatriptan succinate 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.