Manufacturer record

Johnlee Pharmaceuticals Pvt. Ltd: regulatory record

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

2 batches manufactured by Johnlee Pharmaceuticals Pvt. Ltd (Uttarakhand) were declared Not of Standard Quality between February 2024 and April 2024. 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: RDCPH230 02, Cyclosporine Capsules IP 25 mg (Cycloclean- 25) (exp Sep 2025). CDL Kolkata (CDSCO lab) found it not of standard quality: Water. Listed in the April 2024 alert.

Records by type

2 records linked to Johnlee Pharmaceuticals Pvt. Ltd 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
2Failed 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, Feb 2024 to Apr 2024

View original document

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 Always check the linked government document for the current position, and tell us if something is out of date.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

2
NSQ batches since 2024
2
Products affected
Water content
Most common failure
Apr 2024
Latest alert

Flagged batches per year

2024 · 2

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Cyclosporine Capsules IP 25 mg (Cycloclean- 25) Batch RDCPH230 02Mfg Oct 2023 · Exp Sep 2025 WaterWater content CDL KolkataCDSCO lab Apr 2024
Pantoprazole Gastro- resistant Tablets IP (Pantojohn - 20) Batch T-2210131Mfg Oct 2022 · Exp Sep 2025 Dissolution in buffer stageDissolution CDTL MumbaiCDSCO lab Feb 2024

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