Butalbital — Class III drug recall D-0256-2022
Ongoing recall by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals, reported 2021-12-01, distributed nationwide. Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
| Recall number | D-0256-2022 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals, Burbank, CA, United States |
| Recall initiated | 2021-09-28 |
| Classified | 2021-11-23 |
| Reported by FDA | 2021-12-01 |
| Distributed | Nationwide (US) |
| Quantity | 119 bottles |
| Reason classes | labeling |
| NDC | 63629-8392-03, 63629-8392-04, 63629-8392-09 |
| Lot numbers | 151114, 151131, 151160, 151375, 151693, 151708, 151822, 152151, 152156, 152245, 152614, 152838 |
| Expiration dates | 2022-07-31 |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0256-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.