BUPROPION HYDROCHLORIDE
Recalling Firm / Manufacturer: Graviti Pharmaceuticals Private Limited
(Hyderabad, India)
FDA Recall Number: D-0037-2026
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
BUPROPION HYDROCHLORIDE
Generic Name
BUPROPION HYDROCHLORIDE
Active Substance(s)
Bupropion Hydrochloride
Administration Route
Oral
National Drug Code (NDC)
16571-862
Total Quantity Recalled
46,512/30 count bottles
Official Reason for Recall
Specific hazard or quality defect cited by the FDA
According to the official FDA enforcement report:
Failed Tablet/Capsule Specifications
Full Product Description
Packaging specifications and labeling details
Bupropion Hydrochloride Extended-Release Tablets USP (XL), 300 mg, 30-count bottles, Rx Only, Mfd. by: Graviti Pharmaceuticals Private Limited, Sangareddy, Telangana, India, Dist. by: Rising Phar, NDC 16571-863-03.
Enforcement & Regulatory Details
FDA classification, report dates, and initiation authority
Health Hazard Classification
Class II
Current Action Status
Ongoing
FDA Enforcement Report Date
October 29, 2025
Firm Initiation Date
September 15, 2025
FDA Classification Date
Oct 21, 2025
Initiation Type
Voluntary: Firm initiated
Affected Lots & Batch Numbers
Product codes, lot numbers, and expiration dates
Batch # BPB124341A, Exp date: 10/2026
Distribution Information
Geographic scope of affected shipments
Product was distributed to 1 distributor and 16 wholesalers/pharmacy retailers 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-0037-2026
Questo Retrieval Date: July 31, 2026 14:36 1785508611UTCC