SEVELAMER CARBONATE
Summary
FDA approved SEVELAMER CARBONATE by BIONPHARMA. ANDA (Generic) approval (Manufacturing (CMC)) on 2022-01-07. FOR SUSPENSION, ORAL.
Details
Source
Drug Approval
External ID
ANDA209374-1
Action Date
2022-01-07
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
SEVELAMER CARBONATE, FOR SUSPENSION, ORAL. Application: ANDA209374
Company
Context & Analysis
BIONPHARMA has 27 FDA actions in our database.
Frequently Asked Questions
How often does BIONPHARMA have FDA actions?
BIONPHARMA has 27 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 "ANDA209374-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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