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Healthcare Leadership, Policy & Digital Health News India > Blog > Frontline Focus > Telangana Lab Flags 10 Sub-Standard Drugs Two Suppliers Blacklisted from Govt Hospitals

Telangana Lab Flags 10 Sub-Standard Drugs Two Suppliers Blacklisted from Govt Hospitals

Published: October 29, 2025
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A state-run drug testing laboratory in Telangana has identified ten medicines that failed quality tests, leading authorities to blacklist two suppliers for distributing sub-standard products into government hospitals.

Glimpse:

The Central Drugs Standard Control Organisation (CDSCO) surveillance found more than ten drug batches labelled as “Not of Standard Quality” (NSQ) in Telangana, including antibiotics and other essential medicines. Two firms supplying these drugs to government hospitals have been formally blacklisted as a result of the findings.

The Drugs Control Administration of Telangana, working in coordination with the CDSCO, has flagged at least ten drug formulations as sub-standard in recent batch-quality tests. These failures span a variety of medications ranging from antibiotics and painkillers to other essential generics and were identified during scheduled state-level inspections.
As per official records, the drugs failed critical parameters such as assay (active ingredient concentration), dissolution (how the drug releases in the body) and description/presentation (label, packaging standards). These deficiencies raise serious concerns about effectiveness and patient safety.

In response, the state procurement agency for government hospitals (Telangana Medical Services & Infrastructure Development Corporation) has blacklisted two suppliers whose drugs were found to be NSQ, barring them from supplying medicine to government-run health facilities. The action comes amid continuing scrutiny of procured medication quality in public health institutions.
Regulators emphasise that stock of the flagged drugs must be immediately withdrawn from stores, and hospitals have been directed to halt dispensing these batches. Enforcement efforts include show-cause notices, recalls and potential legal action under the Drugs & Cosmetics Act.
Health experts warn that sub-standard medicines reduce therapeutic efficacy, risk antibiotic resistance, prolong illness and impose extra costs on patients and the system. They stress the importance of strengthening quality-control mechanisms at the manufacturing, distribution and hospital procurement stages.

“When essential medicines fail quality tests, we are not just fighting factories we are protecting patients who have no alternative.”

By

HB Team

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