DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE (DEXMEDETOMIDINE HYDROCHLORIDE)
Summary
FDA approved DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE (DEXMEDETOMIDINE HYDROCHLORIDE) by MILLA PHARMS. ANDA (Generic) approval on 2023-06-07. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA217308-1
Action Date
2023-06-07
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE (generic: DEXMEDETOMIDINE HYDROCHLORIDE), INJECTABLE, INJECTION. Application: ANDA217308
Company
Context & Analysis
MILLA PHARMS has 3 FDA actions in our database.
Frequently Asked Questions
How often does MILLA PHARMS have FDA actions?
MILLA PHARMS has 3 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 "ANDA217308-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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