Manufacturer record

Reltsen Health Care: regulatory record

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

2 batches manufactured by Reltsen Health Care (Puducherry) were declared Not of Standard Quality between December 2022 and July 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: R25183701K, Ramipril Tablets IP 5mg (exp Oct 2027). Drugs Testing Laboratory, Madurai-19 (state lab) found it not of standard quality: Ramipril (64.20%). Listed in the July 2026 alert.

Records by type

2 records linked to Reltsen Health Care 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
2Failed 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, Dec 2022 to Jul 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 Always check the linked government document for the current position, and tell us if something is out of date.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.

2
NSQ batches since 2022
2
Products affected
Assay
Most common failure
Jul 2026
Latest alert

Flagged batches per year

2022 · 12026 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Ramipril Tablets IP 5mg Batch R25183701KMfg Nov 2025 · Exp Oct 2027 Ramipril (64.20%)Other Drugs Testing Laboratory, Madurai-19State lab Jul 2026
MYLOMAX (Methylcobalamin, Alpha Lipoic Acid, Folic Acid, Pyridoxine Hydrochloride & Vitamin D3 Tablets) Batch R2295307GMfg Jul 2022 · Exp Dec 2023 Assay of Alpha Lipoic AcidAssay CDL KolkataCDSCO lab Dec 2022

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