RecallRadar

FDA Drug recall D-0455-2017

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)…

On 2017-02-08 the FDA classified a Class II recall of 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)… by Sun Pharmaceutical Industries, citing failed Dissolution Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0455-2017
ClassificationClass II
Statusterminated
Initiated2017-01-12
Published2017-02-08
Last updated2026-09-13 11:51 UTC
CompanySun Pharmaceutical Industries
DistributionUS

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

Failed Dissolution Specifications

Identifiers

ndc62756-517-83
ndc62756-517-88
ndc62756-517-08
ndc62756-517-13
ndc62756-517-18
ndc62756-518-83
ndc62756-518-88
ndc62756-518-08
ndc62756-518-13
ndc62756-518-18
ndc62756-519-83
ndc62756-519-88
ndc62756-519-08
ndc62756-519-13
ndc62756-519-18
ndc62756-985-01
ndc62756-985-02
code_infoa) JKP5530A Exp. 12/17, JKP3991A Exp. 11/17, JKR6535A Exp. 07/18 b) JKP5529A Exp. 11/17

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0455-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.