PlainRecalls
FDA Drug Low Class III Ongoing

Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504.

Reported: December 1, 2021 Initiated: September 28, 2021 #D-0256-2022

Product Description

Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504.

Reason for Recall

Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label

Details

Units Affected
119 Bottles
Distribution
Nationwide in the USA
Location
Burbank, CA

Frequently Asked Questions

What product was recalled?
Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504.. Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals. Units affected: 119 Bottles.
Why was this product recalled?
Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
Which agency issued this recall?
This recall was issued by the FDA Drug on December 1, 2021. Severity: Low. Recall number: D-0256-2022.