BUPROPION HYDROCHLORIDE
Summary
FDA approved BUPROPION HYDROCHLORIDE by SUN PHARM. ANDA (Generic) approval (Labeling) on 2023-10-10. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA203650-2
Action Date
2023-10-10
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
BUPROPION HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA203650
Company
Context & Analysis
SUN PHARM has 48 FDA actions in our database.
Frequently Asked Questions
How often does SUN PHARM have FDA actions?
SUN PHARM has 48 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 "ANDA203650-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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