Bionpharma recalls doxylamine succinate and pyridoxine tablets over foreign tablets or capsules found in bottles
The notice says the 100-count bottles of these delayed-release tablets may contain foreign tablets or capsules, meaning some bottles may hold pills that are not the medicine on the label.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- Product
- Doxylamine 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.
- Company
- Bionpharma Inc.
- Hazard
- Presence of Foreign Tablets/Capsules
- Units
- 14,232 bottles (1,423,200 tablets)
- Where sold
- US Nationwide.
- FDA classification
- Class III · Ongoing
- Classified by FDA
- August 28, 2026
- Recall started
- August 7, 2026
- FDA enforcement report
- September 9, 2026
- Identifiers
- Codes: Lot # DMA25006, Exp Date: 11/30/2028.
- FDA recall number: D-0822-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- Doxylamine 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.
- Reason for recall
- Presence of Foreign Tablets/Capsules
- Classification
- Class III (Ongoing)
- Distribution
- US Nationwide.
- Quantity
- 14,232 bottles (1,423,200 tablets)
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