Manufacturer record
Cosway Pharmaceuticals: regulatory record
Last checked 3 November 2026. Source: CDSCO monthly NSQ alerts and state drug-testing laboratories
2 batches manufactured by Cosway Pharmaceuticals were declared Not of Standard Quality between September 2020 and June 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: CWHC-283, M2 Pan-DSR (Pantoprazole Gastro-resistant & Domperidone Prolonged-release Capsules IP) (exp Sep 2024). State Lab Maharashtra (state lab) found it not of standard quality: THE SAMPLE DOES NOT COMPLY WITH IP REQUIREMENTS FOR DISSOLUTION OF PANTOPRAZOLE AT ACID STAGE. Listed in the June 2024 alert.
Records by type
2 records linked to Cosway 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.
CDSCO drug alerts: Not of Standard Quality and spurious drugs
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 Always check the linked government document for the current position, and tell us if something is out of date.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.
Flagged batches per year
All flagged batches
| Product | Batch | Reason declared NSQ | Tested by | Alert |
|---|---|---|---|---|
| M2 Pan-DSR (Pantoprazole Gastro-resistant & Domperidone Prolonged-release Capsules IP) | Batch CWHC-283Mfg Oct 2022 · Exp Sep 2024 | THE SAMPLE DOES NOT COMPLY WITH IP REQUIREMENTS FOR DISSOLUTION OF PANTOPRAZOLE AT ACID STAGEDissolution | State Lab MaharashtraState lab | Jun 2024 |
| Isopropyl Alcohol, Carbopol, Triethanolamine, Glycerin and Chlorhexidine Digluconate Hand Sanitizer (Safe And Clean Hand Sanitizer) | Batch C-02Mfg Apr 2020 · Exp Mar 2022 | Assay of Glycerin, Chlorhexidine DigluconateAssay | RDTL ChandigarhState lab | Sep 2020 |
Right of reply. Manufacturers may submit a response or a laboratory re-test result; it is published unedited alongside this record. Submit a response.