Class II · Moderate risk
carBAMazepine ER Tablet
Labeling: Label Mixup; carBAMazepine ER Tablet, 200 mg may be potentially mislabeled as ACARBOSE, Tablet, 25 mg, NDC 00054014025, Pedigree: AD60272_1, EXP: 5/22/2014.
National Drug Code
Is NDC 51672-4124-01 recalled?
Carbamazepine · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4124-1)
Yes — this exact package was recalled
1 FDA recall names the code 51672-4124-01 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
- Carbamazepine
- Strength
- CARBAMAZEPINE 200 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 51672-4124
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
- 51672-1386 Fluocinonide 3
- 51672-1351 Ciclopirox 2
- 51672-1385 Ibuprofen 2
- 51672-2130 Ibuprofen 2
- 51672-3007 Hydrocortisone and Acetic Acid 2
- 51672-4005 Carbamazepine 2
Free recall alerts
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