Manufacturer record

Magma Allianz Laboratories Ltd: regulatory record

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

1 batch manufactured by Magma Allianz Laboratories Ltd (Himachal Pradesh) was declared Not of Standard Quality in February 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: MAG-S-1972, Ambroxol Hydrochloride, Levosalbutamol and Guaiphenesin Syrup (Saivent-LX Syrup) (exp Sep 2025). RDTL Chandigarh (CDSCO lab) found it not of standard quality: Assay of Ambroxol Hydrochloride and Levosalbutamol Sulphate calculated as Levosalbutamol. Listed in the February 2024 alert.

Records by type

1 record linked to Magma Allianz Laboratories 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
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, Feb 2024 to Feb 2024

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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 Always check the linked government document for the current position, and tell us if something is out of date.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 2024
1
Products affected
Assay
Most common failure
Feb 2024
Latest alert

Flagged batches per year

2024 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Ambroxol Hydrochloride, Levosalbutamol and Guaiphenesin Syrup (Saivent-LX Syrup) Batch MAG-S-1972Mfg Oct 2023 · Exp Sep 2025 Assay of Ambroxol Hydrochloride and Levosalbutamol Sulphate calculated as LevosalbutamolAssay RDTL ChandigarhCDSCO 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.