Class III · Low risk
Benzonatate Capsules
Superpotent drug: Assay results were slightly above specification at the time zero point.
National Drug Code
Is NDC 68084-0214-11 recalled?
Benzonatate
Yes — this exact package was recalled
2 FDA recalls name the code 68084-0214-11 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
- Benzonatate
- Strength
- BENZONATATE 100 mg/1
- Form
- Capsule · Oral
- Labeler
- American Health Packaging
- Type
- Human Prescription Drug
- Product code
- 68084-0214
Recalls naming this package
Class II · Moderate risk
Benzonatate Capsules
Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
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
- 68084-0295 See recall 3
- 68084-0446 See recall 3
- 68084-0279 See recall 2
- 68084-0325 See recall 2
- 68084-0390 See recall 2
- 68084-0447 See recall 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.