NEOSTIGMINE METHYLSULFATE
Summary
FDA approved NEOSTIGMINE METHYLSULFATE by SAGENT PHARMS INC. ANDA (Generic) approval on 2023-02-17. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
ANDA216542-1
Action Date
2023-02-17
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NEOSTIGMINE METHYLSULFATE, SOLUTION, INTRAVENOUS. Application: ANDA216542
Company
Context & Analysis
SAGENT PHARMS INC has 18 FDA actions in our database.
Frequently Asked Questions
How often does SAGENT PHARMS INC have FDA actions?
SAGENT PHARMS INC has 18 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 "ANDA216542-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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