US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 26, 2019 (7 years ago)

minolira (minocycline hydrochloride) extended-release tablets 135 mg* Physician Sample…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Dissolution Specifications:

What was recalled

minolira (minocycline hydrochloride) extended-release tablets 135 mg* Physician Sample Not for Sale 5 Tablets, Rx Only, Mfg by: Dr. Reddy's Laboratories Limited, FTO-SEZ, Process Unit-01 Devunipalavalasa Village Srikakulam (District) Andhra Pradesh, INDIA. Manufactured for: EPI Health, LLC 134 Columbus St. Charleston, SC 29403 USA. NDC 71403-102-05.

Recalling firm
EPI Health, LLC
NDC code
71403-102-05
Origin
SC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0120-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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