Manufacturer record

Ultra-Chiron Pharmaceuticals Pvt. Ltd: regulatory record

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

2 batches manufactured by Ultra-Chiron Pharmaceuticals Pvt. Ltd (Punjab) were declared Not of Standard Quality between June 2020 and March 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: FRO-1005, Ferrous Ascorbate & Folic Acid Tablets (Faro-XT) (exp Jul 2025). CDL Kolkata (CDSCO lab) found it not of standard quality: Description. Listed in the March 2024 alert.

Records by type

2 records linked to Ultra-Chiron 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
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, Jun 2020 to Mar 2024

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 Always check the linked government document for the current position, and tell us if something is out of date.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

2
NSQ batches since 2020
2
Products affected
Uniformity of weight/content
Most common failure
Mar 2024
Latest alert

Flagged batches per year

2020 · 12024 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Ferrous Ascorbate & Folic Acid Tablets (Faro-XT) Batch FRO-1005Mfg Aug 2023 · Exp Jul 2025 DescriptionDescription CDL KolkataCDSCO lab Mar 2024
Eudox-100 (Doxycycline Capsules I.P.) Batch EDX-1006Mfg Mar 2019 · Exp Feb 2021 Uniformity of WeightUniformity of weight/content CDTL MumbaiCDSCO lab Jun 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.