BUPROPION HYDROCHLORIDE
Summary
FDA approved BUPROPION HYDROCHLORIDE by CHARTWELL RX. ANDA (Generic) approval (Labeling) on 2025-11-06. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA076834-17
Action Date
2025-11-06
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
BUPROPION HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA076834
Company
Context & Analysis
CHARTWELL RX has 64 FDA actions in our database.
Frequently Asked Questions
How often does CHARTWELL RX have FDA actions?
CHARTWELL RX has 64 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA076834-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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