Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg a)… — Class II drug recall D-0455-2017
Terminated recall by Sun Pharmaceutical Industries, Inc., reported 2017-02-08, distributed nationwide. Failed Dissolution Specifications
| Recall number | D-0455-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sun Pharmaceutical Industries, Inc., Cranbury, NJ, United States |
| Recall initiated | 2017-01-12 |
| Classified | 2017-02-02 |
| Reported by FDA | 2017-02-08 |
| Terminated | 2018-06-29 |
| Distributed | Nationwide (US) |
| Quantity | 8,537 bottles |
| Reason classes | specification failure |
| NDC | 62756-0517, 62756-0517-08, 62756-0517-13, 62756-0517-18, 62756-0517-83, 62756-0517-88, 62756-0518, 62756-0518-08, 62756-0518-13, 62756-0518-18, 62756-0518-83, 62756-0518-88, 62756-0519, 62756-0519-08, 62756-0519-13, 62756-0519-18, 62756-0519-83, 62756-0519-88, 62756-0985, 62756-0985-01, 62756-0985-02 |
Product
Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg a) 100-count bottles (NDC 62756-519-88), b) 500-count bottles (NDC 62756-519-13) Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd. Halol-Baroda Highway, Halol-389 350 Gujarat, India.
Reason for recall
Failed Dissolution Specifications
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-0455-2017. 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.