RecallRadar

FDA Drug recall D-0082-2022

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/20 mg, a) 30 count (NDC 43598-744-30), b) 90 count (NDC 43598-744-90) bottles, Rx only…

On 2021-11-10 the FDA classified a Class II recall of Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/20 mg, a) 30 count (NDC 43598-744-30), b) 90 count (NDC 43598-744-90) bottles, Rx only… by Dr Reddy S Laboratories, citing failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0082-2022
ClassificationClass II
Statusterminated
Initiated2021-10-05
Published2021-11-10
Last updated2026-09-13 11:52 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/20 mg, a) 30 count (NDC 43598-744-30), b) 90 count (NDC 43598-744-90) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA

Reason

Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity

Identifiers

ndc43598-742-30
ndc43598-742-90
ndc43598-742-10
ndc43598-744-30
ndc43598-744-90
ndc43598-744-10
ndc43598-743-30
ndc43598-743-90
ndc43598-743-05
ndc43598-745-30
ndc43598-745-90
ndc43598-745-05
code_infoa) L100298 and L100304, exp 01/2023 b) L100235, exp 01/2023

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0082-2022%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.