BUMETANIDE
Summary
FDA approved BUMETANIDE by MANKIND PHARMA. ANDA (Generic) approval on 2025-04-03. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA219291-1
Action Date
2025-04-03
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
BUMETANIDE, TABLET, ORAL. Application: ANDA219291
Company
Context & Analysis
MANKIND PHARMA has 23 FDA actions in our database.
Frequently Asked Questions
How often does MANKIND PHARMA have FDA actions?
MANKIND PHARMA has 23 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 "ANDA219291-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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