GADOTERATE MEGLUMINE
Summary
FDA approved GADOTERATE MEGLUMINE by HENGRUI PHARMA. ANDA (Generic) approval on 2022-04-11. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
ANDA215304-1
Action Date
2022-04-11
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
GADOTERATE MEGLUMINE, SOLUTION, INTRAVENOUS. Application: ANDA215304
Company
Context & Analysis
HENGRUI PHARMA has 6 FDA actions in our database.
Frequently Asked Questions
How often does HENGRUI PHARMA have FDA actions?
HENGRUI PHARMA has 6 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 "ANDA215304-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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