Telangana issues recall for Azima-500 LB tablets over quality concerns

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The Telangana Drug Control Administration and TG SAFE recalled a specific batch of Azima-500 LB tablets after it failed quality testing.
Officials determined the medication was not of standard quality following an analysis at the Central Drugs Laboratory in Kolkata.
Patients are advised to stop using the affected tablets and consult healthcare providers for alternatives.
Retailers and distributors must immediately remove the recalled batch from their inventories and report holdings to local authorities.

Follow-up reporting on whether further batches from J.M. Laboratories are implicated.
Regulatory actions against J.M. Laboratories regarding manufacturing quality standards.

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Named India · Azima-500 LB · Hyderabad · J.M. Laboratories · Solan · Central Drugs Laboratory · Telangana Drug Control Administration · TG SAFE

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