Manufacturer record

Krishna Pharma C-18/5/A: regulatory record

Last checked 3 November 2026. Source: CDSCO monthly NSQ alerts and state drug-testing laboratories

1 batch manufactured by Krishna Pharma C-18/5/A (Telangana) was declared Not of Standard Quality in June 2026. 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: FD4686, Formaldehyde IP Solution (exp Aug 2026). State Lab, DCL, Telangana (state lab) found it not of standard quality: The Sample does not comply test parameter description as it contains white crystals. 2. Label states Formaldehyde I.P solution which is not. Listed in the June 2026 alert.

Records by type

1 record linked to Krishna Pharma C-18/5/A in the datasets we hold. A zero means nothing is on record in those datasets, not that nothing ever happened. What the labels mean.

0Banned or prohibited
0Recalled or suspended
1Failed a lab test
0Regulatory notice
Primary government sourceTier 1: government primary source

CDSCO drug alerts: Not of Standard Quality and spurious drugs

CDSCO · CDSCO monthly NSQ alerts, Jun 2026 to Jun 2026

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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 Always check the linked government document for the current position, and tell us if something is out of date.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.

1
NSQ batches since 2026
1
Products affected
Description
Most common failure
Jun 2026
Latest alert

Flagged batches per year

2026 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Formaldehyde IP Solution Batch FD4686Mfg Sep 2023 · Exp Aug 2026 The Sample does not comply test parameter description as it contains white crystals. 2. Label states Formaldehyde I.P solution which is not availabe in current edition of IP.Description State Lab, DCL, TelanganaState lab Jun 2026

Right of reply. Manufacturers may submit a response or a laboratory re-test result; it is published unedited alongside this record. Submit a response.