ORBACTIV (ORITAVANCIN)
Summary
FDA approved ORBACTIV (ORITAVANCIN) by MELINTA THERAP. NDA (New Drug) approval (Labeling) on 2022-01-14. POWDER, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA206334-7
Action Date
2022-01-14
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ORBACTIV (generic: ORITAVANCIN), POWDER, INTRAVENOUS. Application: NDA206334
Company
Context & Analysis
MELINTA THERAP has 2 FDA actions in our database.
Frequently Asked Questions
How often does MELINTA THERAP have FDA actions?
MELINTA THERAP has 2 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 "NDA206334-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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