← FDA ENFORCEMENT
D-0037-2026Class II

Graviti Pharmaceuticals Private Limited

Recalling firm
Graviti Pharmaceuticals Private Limited
Product type
Drug
Status
Ongoing
Report date
2025-10-29
Distribution
Product was distributed to 1 distributor and 16 wholesalers/pharmacy retailers nationwide.
Product quantity
46,512/30 count bottles
Initiated by
Voluntary: Firm initiated
Reason for recall

Failed Tablet/Capsule Specifications

Product description

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.

Code / lot info

Batch # BPB124341A, Exp date: 10/2026

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.