Manufacturer record

Ravenbhel Healthcare Pvt. Ltd. 16-17: regulatory record

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

3 batches manufactured by Ravenbhel Healthcare Pvt. Ltd. 16-17 (Jammu & Kashmir) were declared Not of Standard Quality between April 2020 and April 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.

Records by type

3 records linked to Ravenbhel Healthcare Pvt. Ltd. 16-17 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
3Failed 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, Apr 2020 to Apr 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 Always check the linked government document for the current position, and tell us if something is out of date.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.

3
NSQ batches since 2020
3
Products affected
Assay
Most common failure
Apr 2026
Latest alert

Flagged batches per year

2020 · 12024 · 12026 · 1

All flagged batches

Product Batch Reason declared NSQ Tested by Alert
Albendazole Tablets IP 400mg 296725043Mfg 2025-04 · Exp 2027-03 The sample does not conform to IP 2022 requirements w.r.t Dissolution TestDissolution DTL,Dalgate Srinagar kashmirState lab Apr 2026
Exudase DP 3023118Mfg 2023-09 · Exp 2025-08 The sample fails in the test, ?Description of tablets?.Description State Drugs Testing Laboratory Srinagar (Jammu & Kashmir)State lab Apr 2024
CDPIN 10 (Cilnidipine Tablets I.P. 10 mg) 549J001Mfg 2019-10 · Exp 2021-03 AssayAssay CDL KolkataCDSCO lab Apr 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.