Manufacturer record

Ramom Healthcare Pvt.Ltd: regulatory record

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

1 batch manufactured by Ramom Healthcare Pvt.Ltd 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 Ramom Healthcare 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

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 Always check the linked government document for the current position, and tell us if something is out of date.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

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

Flagged batches per year

2025 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Omega-3 Fatty Acid, Green Tea Extract, Ginkgo Biloba, Ginseng Extract, Grape Seed Extract, Multimineral, Multivitamin with Antioxidants and Trace Elements Softgel Capsules (VRICH-24 CAPSULES) RHSD-3149FMfg 2024-02 · Exp 2026-01 Assay of Magnesium Oxide calculated as elemental Magnesium, Vitamin D3, Ferrous Fumarate, Zinc Oxide calculated as elemental Zinc, Copper Sulphate Pentahydrate calculated as elemental Copper, Manganese Sulphate calculated as elemental Manganese, Calcium Ascorbate, Citrus Bioflavonoids, Vitamin B6, Folic acidAssay RDTL, ChandigarhCDSCO 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.