Product record
Ibucare Plus: batches declared Not of Standard Quality
Last checked 3 November 2026. Source: CDSCO monthly NSQ alerts, Jan 2019 to Sep 2026
1 batch of products named "Ibucare Plus" (as printed by the testing lab) failed a CDSCO or state drug-testing laboratory test in September 2026. This is a record of specific batches, it does not mean the molecule or every brand is unsafe.
Records by type
1 record linked to Ibucare Plus 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 failed batch is not a verdict on every pack of this product. 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 Always check the linked government document for the current position, and tell us if something is out of date.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
| Batch | Manufacturer | Reason declared NSQ | Tested by | Alert |
|---|---|---|---|---|
| Batch IT6183Mfg May 2026 · Exp Apr 2029 | Inducare Pharmaceutical And Research Foundation Pvt. Ltd. G-32Maharashtra | THE SAMPLE DOES NOT GIVE I.P. IDENTIFICATION TEST FOR THE PRESENCE OF IBUPROFEN. THEREFORE, THE DRUG IS DECLARED AS SPURIOUS VIDE SECTION 17-B OF THE DRUGS AND COSMETICS ACT 1940 AND COSMETICS ACT 1945 THEREUNDER.Identification | FDAL, MumbaiState lab | Sep 2026 |
How to use this. Match the batch number on your strip or bottle against the list. If your batch is listed, return it to the pharmacy and ask for a replacement; if not, the product is not on any alert as of September 2026. Check any batch number.