NAROPIN (ROPIVACAINE HYDROCHLORIDE)
Summary
FDA approved NAROPIN (ROPIVACAINE HYDROCHLORIDE) by FRESENIUS KABI USA. NDA (New Drug) approval (Labeling) on 2022-06-28. SOLUTION, INJECTION.
Details
Source
Drug Approval
External ID
NDA020533-44
Action Date
2022-06-28
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
NAROPIN (generic: ROPIVACAINE HYDROCHLORIDE), SOLUTION, INJECTION. Application: NDA020533
Company
Context & Analysis
FRESENIUS KABI USA has 70 FDA actions in our database.
Frequently Asked Questions
How often does FRESENIUS KABI USA have FDA actions?
FRESENIUS KABI USA has 70 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 "NDA020533-44" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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