Manufacturer record

Zee Laboratories Ltd. Behind 47: regulatory record

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

11 batches manufactured by Zee Laboratories Ltd. Behind 47 (Himachal Pradesh) were declared Not of Standard Quality between July 2021 and February 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: 425-1598, Nicorandil Tablets I.P. 5 mg (exp Jun 2027). CDTL, Hyderabad (CDSCO lab) found it not of standard quality: The sample received does not conform to I.P. 2022 specification with respect to the tests for Dissolution and Assay only. Listed in the February 2026 alert.

Records by type

11 records linked to Zee Laboratories Ltd. Behind 47 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
11Failed 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, Jul 2021 to Feb 2026

View original document

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 Always check the linked government document for the current position, and tell us if something is out of date.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

11
NSQ batches since 2021
9
Products affected
Dissolution
Most common failure
Feb 2026
Latest alert

Flagged batches per year

2021 · 12025 · 92026 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Nicorandil Tablets I.P. 5 mg Batch 425-1598Mfg Jul 2025 · Exp Jun 2027 The sample received does not conform to I.P. 2022 specification with respect to the tests for Dissolution and Assay only.Assay CDTL, HyderabadCDSCO lab Feb 2026
Piperacillin and Tazobactam Injection I.P. 4.5 gm Batch 325-1088Mfg Aug 2025 · Exp Jul 2027 The sample does not conform to claim as per IP 2022 in respect to The Test of Particulate matterParticulate matter RDTL, ChandigarhCDSCO lab Dec 2025
Piperacillin and Tazobactam Injection I.P. 4.5 gm Batch 325-1090Mfg Aug 2025 · Exp Jul 2027 The sample does not conform to claim as per IP 2022 in respect to The Test of Particulate matter.Particulate matter RDTL, ChandigarhCDSCO lab Dec 2025
Sodium Valproate Gastro-resistant Tablets I.P. 200 mg. Batch 425-263Mfg Jan 2025 · Exp Dec 2026 The sample is not of standard quality for the reason stated under "Description" of the tablets.Description RDTL, GuwahatiCDSCO lab Nov 2025
Itraconazole Capsule IP 100mg Batch 1725-230Mfg Apr 2025 · Exp Sep 2027 The sample does not conforrm to the IP with respect to DissolutionDissolution DTL, JaipurState lab Nov 2025
Clopidogrel and Aspirin Tablets IP (75 mg/75 mg) Batch Z24-293Mfg Apr 2024 · Exp Mar 2026 The sample does not conform to I.P with respect to DissolutionDissolution CDL, KolkataCDSCO lab Oct 2025
Amoxycillin & Potassium Clavulanate Injection I.P. Batch 324-869Mfg Jul 2024 · Exp Jun 2026 The sample does not conform to claim as per I.P. 2022 with respect to the test for "Assay" of Amoxycillin and Clavulanic Acid.Assay RDTL, GuwahatiCDSCO lab Oct 2025
Clopidogrel & Aspirin Tablets I.P. (75 mg & 75 mg) Batch Z24-338Mfg May 2024 · Exp Apr 2026 sample does not conform to I.P with respect to the test for Dissolution (Clopidogrel).Dissolution CDTL, IndoreCDSCO lab Sep 2025
Tobramycin Ophthalmic Solution USP 0.3% w/v Batch Z24-506Mfg Jul 2024 · Exp Jun 2026 Assay of TobramycinAssay CDL, KolkataCDSCO lab Aug 2025
Amikacin Sulphate Injection IP 500mg/2ml Batch 325-179Mfg Feb 2025 · Exp Jan 2027 Particulate matter and DescriptionDescription CDL, KolkataCDSCO lab Aug 2025
(Levoziv -500) Levofloxacin Tablets I.P. 500 mg Batch 420-1087Mfg Jul 2020 · Exp Jun 2023 DissolutionDissolution RDTL GuwahatiState lab Jul 2021

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