Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals recalls Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode 083929164865; b) 2…

Recall date

September 28, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0257-2022

FDA classification

Class III

Brand / firm

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Sold / distributed

Nationwide in the USA

Why it was recalled

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

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode 083929164865; b) 20-count bottles, NDC: 71335-1767-01, barcode 083921157837; c) 30-count bottles, NDC: 71335-1767-02, barcode 083922165687, d) 60-count bottles, NDC: 71335-1767-03, barcode 083923153776, e) 90-count bottles, NDC: 71335-1767-04, barcode 083924152889, f) 120-count bottles, NDC: 71335-1767-07, barcode 083927153735. Westminster Pharmaceuticals LLC, Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504 USA