Manufacturer record

Marvellon Pharmaceuticals Pvt. Ltd: regulatory record

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

3 batches manufactured by Marvellon Pharmaceuticals Pvt. Ltd (Himachal Pradesh) were declared Not of Standard Quality between November 2025 and 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.

Records by type

3 records linked to Marvellon 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
3Failed 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, Nov 2025 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 Always check the linked government document for the current position, and tell us if something is out of date.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.

3
NSQ batches since 2025
3
Products affected
Other
Most common failure
Jun 2026
Latest alert

Flagged batches per year

2025 · 12026 · 2

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Promethazine Hydrochloride Syrup IP MDL-C819Mfg 2025-12 · Exp 2027-11 ContentOther DTL, Chennai-06State lab Jun 2026
Ambroxol Hydrochloride, Terbutaline Sulphate and Guaiphenesin Syrup & Menthol Syrup MDL-B458Mfg 2024-09 · Exp 2026-08 The sample does not conform to the claim with respect to In Assay Terbutaline Sulphate, Ambroxol Hydrochloride and Guaiphenesin.Assay DTL JaipurState lab Jan 2026
�(Cyproheptadine Hydrochloride & Tricholine Citrate syrup) MDL-B641Mfg 2024-11 · Exp 2026-10 ContentOther Drugs Testing Laboratory, Madurai-19State lab Nov 2025

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