NALOXONE HYDROCHLORIDE
Summary
FDA approved NALOXONE HYDROCHLORIDE by BAXTER HLTHCARE CORP. ANDA (Generic) approval (Labeling) on 2024-08-28. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA214785-4
Action Date
2024-08-28
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NALOXONE HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA214785
Company
Context & Analysis
BAXTER HLTHCARE CORP has 15 FDA actions in our database.
Frequently Asked Questions
How often does BAXTER HLTHCARE CORP have FDA actions?
BAXTER HLTHCARE CORP has 15 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 "ANDA214785-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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