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Class II: temporary or reversible health riskOngoing

Preferred Pharmaceuticals Ondansetron ODT Tablets Recall

Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceutical…

Preferred Pharmaceuticals, Inc. · Anaheim, CA

Risk level
Class II
Reported by FDA
Dec 24, 2025
Recall ID
D-0239-2026
Check your lot numberHow we source this data

Summary

Preferred Pharmaceuticals recalled Ondansetron ODT Tablets starting Nov 17, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0239-2026 on Dec 24, 2025. Reason: Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale. Status: Ongoing.

Why it was recalled

Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.

Product description

Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged by Preferred Pharmaceuticals NDC 68788-8666-01

Lot numbers, UPCs & expiration codes

Lot: J1325J, I1725P, EXP Date: 4/30/2027.

Where it was sold

Natinowide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0239-2026
Classification
Class II
Status
Ongoing
Recall initiated
Nov 17, 2025
FDA report date
Dec 24, 2025
Quantity
575 1x10 Foil Blister Packs
Recall type
Voluntary: Firm initiated
Recalling firm
Preferred Pharmaceuticals, Inc.

Original FDA data

Every field from FDA enforcement report D-0239-2026, exactly as published.

Show all FDA fields
City
Anaheim
State
CA
Status
Ongoing
Country
United States
Event ID
98141
Address
1250 N Lakeview Ave Ste O
Code information
Lot: J1325J, I1725P, EXP Date: 4/30/2027.
Postal code
92807-1801
Report date
Dec 24, 2025
Product type
Drugs
Recall number
D-0239-2026
Classification
Class II
Recalling firm
Preferred Pharmaceuticals, Inc.
Product quantity
575 1x10 Foil Blister Packs
Reason for recall
Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged by Preferred Pharmaceuticals NDC 68788-8666-01
Distribution pattern
Natinowide in the USA
Recall initiation date
Nov 17, 2025
Initial firm notification
Letter
Center classification date
Dec 17, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0239-2026, published Dec 24, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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