TIMOLOL MALEATE
Recalling Firm / Manufacturer: FDC Limited
(Aurangabad, Maharashtra State, India)
FDA Recall Number: D-0543-2025
Source Authority Disclaimer: This drug recall notice is published by Questo using official enforcement reports issued by the U.S. Food & Drug Administration (FDA). It is provided for informational, academic, and clinical research purposes only. Patients should not discontinue prescribed treatments without consulting their physician or pharmacist.
Product & Identification Information
Brand, active ingredients, NDC codes, and manufacturer details
Brand / Trade Name
TIMOLOL MALEATE
Generic Name
TIMOLOL MALEATE
Active Substance(s)
Timolol Maleate
Administration Route
Ophthalmic
National Drug Code (NDC)
64980-513
Total Quantity Recalled
154,176 bottles
Official Reason for Recall
Specific hazard or quality defect cited by the FDA
According to the official FDA enforcement report:
Defective Container: spike of the cap becomes lodged in the nozzle of the product bottle.
Full Product Description
Packaging specifications and labeling details
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-05.
Enforcement & Regulatory Details
FDA classification, report dates, and initiation authority
Health Hazard Classification
Class II
Current Action Status
Ongoing
FDA Enforcement Report Date
August 06, 2025
Firm Initiation Date
July 05, 2025
FDA Classification Date
Jul 29, 2025
Initiation Type
Voluntary: Firm initiated
Affected Lots & Batch Numbers
Product codes, lot numbers, and expiration dates
Lot#: 083L061, Exp.: 11/2025.
Distribution Information
Geographic scope of affected shipments
U.S Nationwide.
Safety Guidance & Actions
Standard FDA protocol for patients and healthcare providers
Patient Advisory
Check your prescription bottle or packaging against the affected lot numbers listed above. If your medication matches a recalled lot, contact your pharmacist for replacement guidance.
Healthcare Provider Guidance
Audit pharmacy stock and return affected lots to the distributor per manufacturer instructions. Notify patients where clinically indicated.
Official Source Provenance
Verified regulatory citation from U.S. FDA OpenFDA
Primary Data Source: U.S. Food & Drug Administration (FDA) OpenFDA API
Recall Number: D-0543-2025
Questo Retrieval Date: July 31, 2026 14:36 1785508615UTCC