Manufacturer record

Ridley Lifescience Pvt. Ltd: regulatory record

Last checked 20 September 2026. Source: CDSCO monthly NSQ alerts and state drug-testing laboratories

4 batches manufactured by Ridley Lifescience Pvt. Ltd (Delhi) were declared Not of Standard Quality between April 2022 and August 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.

Records by type

4 records linked to Ridley Lifescience 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
4Failed 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, Apr 2022 to Aug 2025

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 Always check the linked government document for the current position, and tell us if something is out of date.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

4
NSQ batches since 2022
4
Products affected
Assay
Most common failure
Aug 2025
Latest alert

Flagged batches per year

2022 · 12023 · 22025 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Ciprofloxacin Tablets IP 500 mg RT230545Mfg 2023-07 · Exp 2026-06 Assay & DissolutionAssay State Drugs Testing Laboratory, Govt. of Tripura, AgartalaCDSCO lab Aug 2025
PHENIRAMINE MALEATE TABLETS IP (APVIL) APV-2001Mfg 2020-12 · Exp 2023-11 Description, Uniformity of Weight and AssayAssay CDTL HyderabadCDSCO lab Feb 2023
Misoprostol Tablets I.P. 200 mcg RT220304Mfg 2022-03 · Exp 2024-02 AssayAssay CDL KolkataCDSCO lab Jan 2023
Ampicillin Capsules IP AMI-1901Mfg 2019-07 · Exp 2022-06 Assay and MisbrandedAssay RDTL GuwahatiState lab Apr 2022

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