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Class III · Lower riskActive recall

Doxylamine Succinate And Pyridoxine Hydrochloride

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot # DMA25006, Exp Date: 11/30/2028.
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Foreign Tablets/Capsules

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMade in INDIA foreign manufacturer
Brand nameDOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE
Generic nameDOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE
Active ingredient(s)DOXYLAMINE SUCCINATE, PYRIDOXINE HYDROCHLORIDE
Distributed by / forBionpharma Inc., Princeton, NJ 08540
NDC69452-206-20
Show the full FDA record
Full product labelDoxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg, 100-count bottle, Rx Only, MADE IN INDIA, Distributed by: Bionpharma Inc., Princeton, NJ 08540 NDC 69452-206-20.
Recalling firmBionpharma Inc.
DistributionUS Nationwide.
Quantity14,232 bottles (1,423,200 tablets)
Recall initiated2026-08-07
Report date2026-09-09
Recall completed
Recall numberD-0822-2026
ClassificationClass III
FDA statusOngoing
Origin on filePrinceton NJ United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.