RecallRadar

FDA Drug recall D-1381-2014

Dr. Reddy's Metoprolol Succinate Extended Release Tablets, USP 25 mg. 100-count bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories…

On 2014-06-18 the FDA classified a Class II recall of Dr. Reddy's Metoprolol Succinate Extended Release Tablets, USP 25 mg. 100-count bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories… by Dr Reddy S Laboratories, citing failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1381-2014
ClassificationClass II
Statusterminated
Initiated2014-05-23
Published2014-06-18
Last updated2026-09-13 11:51 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

Dr. Reddy's Metoprolol Succinate Extended Release Tablets, USP 25 mg. 100-count bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories Limited, Batchupally - 500 090 India. NDC55111-466-01

Reason

Failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point.

Identifiers

ndc55111-466-30
ndc55111-466-60
ndc55111-466-01
ndc55111-466-05
ndc55111-466-79
ndc55111-466-78
ndc55111-467-30
ndc55111-467-60
ndc55111-467-01
ndc55111-467-05
ndc55111-467-79
ndc55111-467-78
code_infoLot # C206578 Exp. 05/2014 Lot # C207415 Exp. 06/2014

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-1381-2014%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.