NEOSTIGMINE METHYLSULFATE
Summary
FDA approved NEOSTIGMINE METHYLSULFATE by BE PHARMS. ANDA (Generic) approval (Labeling) on 2022-05-10. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
ANDA212512-1
Action Date
2022-05-10
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NEOSTIGMINE METHYLSULFATE, SOLUTION, INTRAVENOUS. Application: ANDA212512
Company
Context & Analysis
BE PHARMS has 4 FDA actions in our database.
Frequently Asked Questions
How often does BE PHARMS have FDA actions?
BE PHARMS has 4 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 "ANDA212512-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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