Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose)
Reported: April 8, 2015 Initiated: January 6, 2015 #D-0430-2015
Product Description
Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose)
Reason for Recall
Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
Details
- Recalling Firm
- American Health Packaging
- Units Affected
- 2284 cartons (100 individual unit doses per carton)
- Distribution
- Nationwide
- Location
- Columbus, OH
Frequently Asked Questions
What product was recalled? ▼
Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose). Recalled by American Health Packaging. Units affected: 2284 cartons (100 individual unit doses per carton).
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 8, 2015. Severity: Moderate. Recall number: D-0430-2015.
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