Class II · Moderate risk
Oxcarbazepine Tablets 600mg
Presence of foreign substance
National Drug Code
Is NDC 62756-0185-18 recalled?
Oxcarbazepine · 1000 TABLET, FILM COATED in 1 BOTTLE (62756-185-18)
Yes — this exact package was recalled
1 FDA recall names the code 62756-0185-18 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 600 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 62756-0185
Recalls naming this package
Class II · Moderate risk
OXcarbazepine Tablet
Labeling:Label Mixup; OXcarbazepine Tablet, 600 mg may be potentially mislabeled as LACTASE ENZYME, Tablet, 3000 units, NDC 24385014976, Pedigree: AD30028_25, EXP: 5/7/2014.
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
- 62756-0233 Amphotericin B 2
- 62756-0522 sumatriptan succinate 2
- 62756-0551 See recall 2
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