Manufacturer record
Caspian Pharmaceuticals: regulatory record
Last checked 20 September 2026. Source: CDSCO monthly NSQ alerts and state drug-testing laboratories
4 batches manufactured by Caspian Pharmaceuticals (Himachal Pradesh) were declared Not of Standard Quality between April 2024 and May 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
4 records linked to Caspian Pharmaceuticals in the datasets we hold. A zero means nothing is on record in those datasets, not that nothing ever happened. What the labels mean.
CDSCO drug alerts: Not of Standard Quality and spurious drugs
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 Always check the linked government document for the current position, and tell us if something is out of date.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.
Flagged batches per year
All flagged batches
| Product | Batch | Reason declared NSQ | Tested by | Alert |
|---|---|---|---|---|
| Vitamin E Acetate Soft Gelatin Caspules | D26SBM07Mfg 2026-03 · Exp 2028-02 | The Product is official in USP Which is not Printed on the strips as required under the Act.Other | SDTL, PunjabState lab | May 2026 |
| Vitamin E Acetate Soft Gelatin Caspules | D26SBM08Mfg 2026-03 · Exp 2028-02 | The Product is official in USP Which is not Printed on the strips as required under the Act.Other | SDTL, PunjabState lab | May 2026 |
| Vitamin E Acetate Soft Gelatin Caspules | D26SBM05Mfg 2026-03 · Exp 2028-02 | The Product is official in USP Which is not Printed on the strips as required under the Act.Other | SDTL, PunjabState lab | May 2026 |
| Diphenhydramine Hydrochloride Capsules IP (XL Dryl-D Capsules) | CPD240100 6Mfg 2024-01 · Exp 2025-12 | Dissolution and Assay of Diphenhydramin e HydrochlorideAssay | RDTL ChandigarhCDSCO lab | Apr 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.