Belladonna Alkaloids with Phenobarbital Tablets — Class II drug recall D-883-2013
Terminated recall by West-Ward Pharmaceutical Corp., reported 2013-08-21, distributed nationwide. Presence of Foreign Substance: black specks comprised of degraded organic material found on tablets
| Recall number | D-883-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | West-Ward Pharmaceutical Corp., Eatontown, NJ, United States |
| Recall initiated | 2013-07-30 |
| Classified | 2013-08-12 |
| Reported by FDA | 2013-08-21 |
| Terminated | 2014-06-23 |
| Distributed | Nationwide (US) |
| NDC | 00143-1140-10, 00143-1140-51 |
| Lot numbers | 67328A, 67329A, 67330B, 67330C, 68064A, 68064B, 68065A, 68666A, 68666B, 68667A, 69721A, 69722A |
| Model numbers | 1140-10, 1140-51 |
Product
Belladonna Alkaloids with Phenobarbital Tablets, 1000 count (NDC 0143-1140-10) and 5000 count (NDC 0143-1140-51) PET bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp., Eatontown, N.J., 07724.
Reason for recall
Presence of Foreign Substance: black specks comprised of degraded organic material found on tablets
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-883-2013. 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.