Manufacturer record

MMG Healthcare: regulatory record

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

3 batches manufactured by MMG Healthcare (Himachal Pradesh) were declared Not of Standard Quality between May 2019 and January 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 MMG Healthcare 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, May 2019 to Jan 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 Always check the linked government document for the current position, and tell us if something is out of date.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 2019
3
Products affected
Particulate matter
Most common failure
Jan 2026
Latest alert

Flagged batches per year

2019 · 12025 · 12026 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Pantoprazole for Injection IP 40 mg 25GF05AMfg 2025-06 · Exp 2027-05 The sample does not conform to I.P. with respect to test for Particulate matter, and Clarity of solutionParticulate matter CDL, KolkataCDSCO lab Jan 2026
Ceftriaxone and Sulbactam for Injection IP (CEFRITZ S 1.5) 24DH13VMfg 2024-08 · Exp 2026-07 Bacterial endotoxins for Sterile water for Injection.Water content CDL KolkataCDSCO lab Apr 2025
Herzovir Lyophillized Powder (Aciclovir Intravenous Infusion I.P.) GN1310AMfg 2017-11 · Exp 2019-10 Particulate MatterParticulate matter CDL KolkataCDSCO lab May 2019

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