PREVDUO (NEOSTIGMINE METHYLSULFATE AND GLYCOPYRROLATE)
Summary
FDA approved PREVDUO (NEOSTIGMINE METHYLSULFATE AND GLYCOPYRROLATE) by AZURITY. NDA (New Drug) approval (New Combination and New Formulation or New Manufacturer) on 2023-02-23. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA216903-1
Action Date
2023-02-23
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
PREVDUO (generic: NEOSTIGMINE METHYLSULFATE AND GLYCOPYRROLATE), SOLUTION, INTRAVENOUS. Application: NDA216903
Company
Context & Analysis
AZURITY has 21 FDA actions in our database.
Frequently Asked Questions
How often does AZURITY have FDA actions?
AZURITY has 21 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 "NDA216903-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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