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Class II: temporary or reversible health riskOngoing

Glenmark Pharmaceuticals Fluphenazine Hydrochloride Tablets 2 Recall

Fluphenazine Hydrochloride Tablets 2

Glenmark Pharmaceuticals Inc., USA · Mahwah, NJ

Risk level
Class II
Reported by FDA
Apr 16, 2025
Recall ID
D-0327-2025
Check your lot numberHow we source this data

Summary

Glenmark Pharmaceuticals recalled Fluphenazine Hydrochloride Tablets 2 starting Mar 13, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0327-2025 on Apr 16, 2025. Reason: CGMP Deviations. Status: Ongoing.

Why it was recalled

CGMP Deviations

Product description

Fluphenazine Hydrochloride Tablets 2.5mg, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430. NDC# 68462-336-01

Lot numbers, UPCs & expiration codes

Lot # 17232214, exp. date Sep-25

Where it was sold

U.S. Nationwide

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-0327-2025
Classification
Class II
Status
Ongoing
Recall initiated
Mar 13, 2025
FDA report date
Apr 16, 2025
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Glenmark Pharmaceuticals Inc., USA

Original FDA data

Every field from FDA enforcement report D-0327-2025, exactly as published.

Show all FDA fields
City
Mahwah
State
NJ
Status
Ongoing
Country
United States
Event ID
96474
Address
750 Corporate Dr
Code information
Lot # 17232214, exp. date Sep-25
Postal code
07430-2009
Report date
Apr 16, 2025
Product type
Drugs
Recall number
D-0327-2025
Classification
Class II
Recalling firm
Glenmark Pharmaceuticals Inc., USA
Reason for recall
CGMP Deviations
Voluntary / mandated
Voluntary: Firm initiated
Product description
Fluphenazine Hydrochloride Tablets 2.5mg, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430. NDC# 68462-336-01
Distribution pattern
U.S. Nationwide
Recall initiation date
Mar 13, 2025
Initial firm notification
Letter
Center classification date
Apr 8, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0327-2025, published Apr 16, 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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