SANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE)
Summary
FDA approved SANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) by NOVARTIS. NDA (New Drug) approval (Labeling) on 2024-07-11. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
NDA021008-49
Action Date
2024-07-11
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
SANDOSTATIN LAR DEPOT (generic: OCTREOTIDE ACETATE), INJECTABLE, INJECTION. Application: NDA021008
Company
Context & Analysis
NOVARTIS has 22 FDA actions in our database.
Frequently Asked Questions
How often does NOVARTIS have FDA actions?
NOVARTIS has 22 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 "NDA021008-49" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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