Manufacturer record

Aban Pharmaceuticals: regulatory record

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

8 batches manufactured by Aban Pharmaceuticals (Kerala) were declared Not of Standard Quality between September 2023 and August 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.

Most recent flagged batch: 25010040, Diclofenac Potass um & Serratiopeptidase Tablets (exp Nov 2027). SDTL, Andhra Pradesh (state lab) found it not of standard quality: The Sample does not confirm to the standards of Disintegration Test mentioned under General Requirements of IP as per Standards for Patent. Listed in the August 2026 alert.

Records by type

8 records linked to Aban Pharmaceuticals 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
8Failed 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, Sep 2023 to Aug 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 Always check the linked government document for the current position, and tell us if something is out of date.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.

8
NSQ batches since 2023
6
Products affected
Dissolution
Most common failure
Aug 2026
Latest alert

Flagged batches per year

2023 · 12024 · 12025 · 22026 · 4

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Diclofenac Potass um & Serratiopeptidase Tablets Batch 25010040Mfg Oct 2025 · Exp Nov 2027 The Sample does not confirm to the standards of Disintegration Test mentioned under General Requirements of IP as per Standards for Patent and Proprietary Medicines in Schedule-V of Drugs and Cosmetics Act, 1940 and Rules there under.Disintegration SDTL, Andhra PradeshState lab Aug 2026
Dextromethorphan Hydrobromide, Chlorpheniramine Maleate & Phenylephrine Hydrochloride Syrup Batch S-199/25Mfg Jul 2025 · Exp Jun 2027 Dextromethorphan Hydrobromide contentOther FDL, VadodaraState lab Jun 2026
Paracetamol Tablets IP Batch 2506006Mfg Jun 2025 · Exp May 2028 The samole does not comply with IP requirment for the Dissolution test.Dissolution FDAL, MumbaiState lab Apr 2026
Paracetamol Tablets I.P. 650 mg Batch 2309026Mfg Sep 2023 · Exp Aug 2026 The sample does not conform to standard quality in respect of the test for Dissolution performed.Dissolution SDTL Govt. of Tripura, AgartalaState lab Jan 2026
Omeprazole Capsule IP 20 mg Batch 153/25Mfg Jan 2025 · Exp Dec 2026 Dissolution (Buffer satage)Dissolution Food & Drugs Laboratory, VadodaraState lab Nov 2025
Paracetamol Tablets I.P 650 mg (Alpa-650 Tablets) Batch 2501032Mfg Jan 2025 · Exp Dec 2027 Test for Dissolution of TabletsDissolution DTL, Bengaluru, KarnatakaState lab Oct 2025
Levocetirizin Hydrochloride &Montelukast Sodium Tablets IP (Montefirst- LC) Batch 2405097Mfg May 2024 · Exp Apr 2026 Test for Dissolution of Levocetirizine Hydrochloride and MontelukastDissolution State Lab KarnatakaState lab Dec 2024
LEVOCETIRIZINE HYDROCHLORIDE TABLETS I.P. 5 mg. (Alocet) Batch 2303117Mfg Mar 2023 · Exp Feb 2026 Assay /Content of Levocetirizin HydrochlorideAssay RDTL GuwahatiState lab Sep 2023

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