Product record

Buprenorphine Hci Naloxone Sublingula: 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 "Buprenorphine Hci Naloxone Sublingula" (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 Buprenorphine Hci Naloxone Sublingula 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, Sep 2026 to Sep 2026

View original document

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 Always check the linked government document for the current position, and tell us if something is out of date.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

1
NSQ batches
1
Manufacturers
Labelling
Most common reason
Sep 2026
Latest alert

Flagged batches

Batch Manufacturer Reason declared NSQ Tested by Alert
Batch SLTE26026Mfg May 2026 · Exp Apr 2028 Swift Life Sciences Pvt. LtdUttarakhand The content of Buprenorphine found to be 0.451 mg per tablet (112.75%) against labelled claim of 0.4 mg per tabletLabelling SDTL, PunjabState 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.