Manufacturer record
BRIT Lifescience a GMP Certified Company) Sainwala kaula Wata: regulatory record
Last checked 3 November 2026. Source: CDSCO monthly NSQ alerts and state drug-testing laboratories
1 batch manufactured by BRIT Lifescience a GMP Certified Company) Sainwala kaula Wata (Himachal Pradesh) was declared Not of Standard Quality in April 2025. Records are batch-specific findings by government laboratories as published in CDSCO's monthly alerts; where a company has stated that a flagged batch was counterfeit, that statement is noted when reported.
Most recent flagged batch: BLT23348, Telivi-H 40 (Telmisartan & Hydrochorothiazide Tablets IP (exp May 2025). CDTL Mumbai (CDSCO lab) found it not of standard quality: 1. The content of Telmisartan and Hydrochlorothiazide in the sample is less (i.e. 83.13% and 79.44%of the labelled amount respectively) than. Listed in the April 2025 alert.
Records by type
1 record linked to BRIT Lifescience a GMP Certified Company) Sainwala kaula Wata in the datasets we hold. A zero means nothing is on record in those datasets, not that nothing ever happened. What the labels mean.
CDSCO drug alerts: Not of Standard Quality and spurious drugs
Scope. A company appearing here is not a finding that its products are unsafe. Regulatory actions can apply to one batch, one formulation, one period or one state. Always check the linked government document for the current position, and tell us if something is out of date. How we label records.
Flagged batches per year
All flagged batches
| Product | Batch | Reason declared NSQ | Tested by | Alert |
|---|---|---|---|---|
| Telivi-H 40 (Telmisartan & Hydrochorothiazide Tablets IP | Batch BLT23348Mfg Jun 2023 · Exp May 2025 | 1. The content of Telmisartan and Hydrochlorothiazide in the sample is less (i.e. 83.13% and 79.44%of the labelled amount respectively) than I.P. limits. 2. The sample does not comply with I.P. Requirements for "Dissolution Test" for Telemisartan and Hydrochlorothiazide.Dissolution | CDTL MumbaiCDSCO lab | Apr 2025 |
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