BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10
Reported: July 5, 2017 Initiated: May 30, 2017 #D-0928-2017
Product Description
BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10
Reason for Recall
Failed Moisture Limits: Product tested out-of-specification for moisture content.
Details
- Recalling Firm
- Mckesson Packaging Services
- Units Affected
- 942 cartons
- Distribution
- Nationwide in the US
- Location
- Concord, NC
Frequently Asked Questions
What product was recalled? ▼
BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10. Recalled by Mckesson Packaging Services. Units affected: 942 cartons.
Why was this product recalled? ▼
Failed Moisture Limits: Product tested out-of-specification for moisture content.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 5, 2017. Severity: Low. Recall number: D-0928-2017.
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