Manufacturer record

Twins Pharma: regulatory record

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

2 batches manufactured by Twins Pharma (Telangana) were declared Not of Standard Quality between November 2024 and June 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

2 records linked to Twins Pharma 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, Nov 2024 to Jun 2025

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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 Always check the linked government document for the current position, and tell us if something is out of date.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 2024
2
Products affected
Dissolution
Most common failure
Jun 2025
Latest alert

Flagged batches per year

2024 · 12025 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Calgro-D3 Tablets Calcium and Vitamin D3 tablets AC.2412Mfg 2024-12 · Exp 2026-05 1. The label should be mentioned as Calcium And Vitamin D3 IP. But the letters IP is not mentioned after the product name. 2. Dissolution for Calcium.Dissolution State Lab Drugs Control Laboratory, TelanganaState lab Jun 2025
Ferin-XT Tafblets, Ferrous Ascorbate, Folic Acid & Zinc Tablets NC.2403Mfg 2024-03 · Exp 2025-08 NOT OF STANDARD QUALITY Sample does not meets the Specifications wrt. Assay of Ferrous Ascorbate (Elemental Iron) as per STPAssay State Lab Drugs Control Laboratory, TelanganaState lab Nov 2024

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