Class II · Moderate risk
Carbamazepine Extended-Release Tablets
Failed Dissolution Specifications.
National Drug Code
Is NDC 60687-0594-21 recalled?
Carbamazepine · 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-594-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-594-11)
Yes — this exact package was recalled
1 FDA recall names the code 60687-0594-21 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.
1 of these recalls is still ongoing.
- Active ingredient
- Carbamazepine
- Strength
- CARBAMAZEPINE 400 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- American Health Packaging
- Type
- Human Prescription Drug
- Product code
- 60687-0594
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
- 60687-0423 Clobazam 2
- 60687-0695 See recall 2
- 60687-0106 See recall 1
- 60687-0112 Anastrozole 1
- 60687-0133 See recall 1
- 60687-0139 See recall 1
Free recall alerts
Know the day your medication is recalled
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