RecallRadar

FDA Drug recall D-0075-2021

Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg, 100-count carton (10 x10 unit-dose), Rx only, Manufactured by: Cadila Hea…

On 2020-11-11 the FDA classified a Class II recall of Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg, 100-count carton (10 x10 unit-dose), Rx only, Manufactured by: Cadila Hea… by Zydus Pharmaceuticals Usa, citing failed Dissolution Specification.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0075-2021
ClassificationClass II
Statusterminated
Initiated2020-10-27
Published2020-11-11
Last updated2026-09-13 11:52 UTC
CompanyZydus Pharmaceuticals Usa
DistributionUS

Product

Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg, 100-count carton (10 x10 unit-dose), Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534, NDC 68382-772-77

Reason

Failed Dissolution Specification

Identifiers

ndc68382-771-30
ndc68382-771-77
ndc68382-772-30
ndc68382-772-77
code_infoLot # M005682, EXP 3/2022

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-0075-2021%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.