Manufacturer record

Mfg By: M/s. Swefn Pharmaceuticals Pvt.Ltd: regulatory record

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

1 batch manufactured by Mfg By: M/s. Swefn Pharmaceuticals Pvt.Ltd (Gujarat) were declared Not of Standard Quality between March 2025 and March 2025. 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

1 record linked to Mfg By: M/s. Swefn 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
1Failed 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, Mar 2025 to Mar 2025

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 Always check the linked government document for the current position, and tell us if something is out of date.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

1
NSQ batches since 2025
1
Products affected
Misbranded
Most common failure
Mar 2025
Latest alert

Flagged batches per year

2025 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Mefifresh Tablets, Mefenamic Acid & Dicyclomine Hydrochloride Tablets, T09243 9Mfg 2024-09 · Exp 2027-08 MISBRANDED The drug product Mefenamic Acid and Dicyclomine HCL tablets is official in Indian Pharmacopoeia. But the letters IP is not mentioned on the strip after the product name Mefenamic Acid and Dicyclomine HCL tablets. Hence it is Misbranded drug under section 17 of Drugs and Cosmetics Act, 1940.Misbranded State Lab, Drugs Control Laboratory, TelanganaState lab Mar 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.