BUPROPION HYDROCHLORIDE XL (BUPROPION HYDROCHLORIDE)
Summary
FDA approved BUPROPION HYDROCHLORIDE XL (BUPROPION HYDROCHLORIDE) by ANBISON LAB. ANDA (Generic) approval (Labeling) on 2024-10-07. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA207224-7
Action Date
2024-10-07
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
BUPROPION HYDROCHLORIDE XL (generic: BUPROPION HYDROCHLORIDE), TABLET, EXTENDED RELEASE, ORAL. Application: ANDA207224
Company
Context & Analysis
ANBISON LAB has 3 FDA actions in our database.
Frequently Asked Questions
How often does ANBISON LAB have FDA actions?
ANBISON LAB has 3 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 "ANDA207224-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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