MELPHALAN HYDROCHLORIDE
Summary
FDA approved MELPHALAN HYDROCHLORIDE by ACTAVIS LLC. ANDA (Generic) approval (Labeling) on 2023-05-15. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA206018-2
Action Date
2023-05-15
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
MELPHALAN HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA206018
Company
Context & Analysis
ACTAVIS LLC has 3 FDA actions in our database.
Frequently Asked Questions
How often does ACTAVIS LLC have FDA actions?
ACTAVIS LLC 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 "ANDA206018-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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