MAGNESIUM SULFATE (MAGNESIUM SULFATE HEPTAHYDRATE)
Summary
FDA approved MAGNESIUM SULFATE (MAGNESIUM SULFATE HEPTAHYDRATE) by ASPIRO. ANDA (Generic) approval on 2025-05-28. SOLUTION, INTRAMUSCULAR, INTRAVENOUS.
Details
Source
Drug Approval
External ID
ANDA219777-1
Action Date
2025-05-28
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
MAGNESIUM SULFATE (generic: MAGNESIUM SULFATE HEPTAHYDRATE), SOLUTION, INTRAMUSCULAR, INTRAVENOUS. Application: ANDA219777
Company
Context & Analysis
ASPIRO has 12 FDA actions in our database.
Frequently Asked Questions
How often does ASPIRO have FDA actions?
ASPIRO has 12 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 "ANDA219777-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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