RecallRadar

FDA Drug recall D-1317-2020

Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals Ltd, Bharuch 392130, I…

On 2020-06-10 the FDA classified a Class II recall of Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals Ltd, Bharuch 392130, I… by Torrent Pharma, citing failed Dissolution Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1317-2020
ClassificationClass II
Statusterminated
Initiated2020-05-11
Published2020-06-10
Last updated2026-09-13 11:52 UTC
CompanyTorrent Pharma
DistributionUS

Product

Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals Ltd, Bharuch 392130, India; Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920, NDC 13668-268-05

Reason

Failed Dissolution Specifications

Identifiers

ndc13668-268-30
ndc13668-268-01
ndc13668-268-10
ndc13668-268-31
ndc13668-268-05
ndc13668-271-01
ndc13668-271-10
ndc13668-271-49
ndc13668-271-05
code_infoLot #: 4FF4F001, Exp 1/2023

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-1317-2020%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.