SUSTOL (GRANISETRON)
Summary
FDA approved SUSTOL (GRANISETRON) by HERON THERAPS INC. NDA (New Drug) approval (Labeling) on 2026-02-23. INJECTABLE, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
NDA022445-14
Action Date
2026-02-23
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
SUSTOL (generic: GRANISETRON), INJECTABLE, SUBCUTANEOUS. Application: NDA022445
Company
Context & Analysis
HERON THERAPS INC has 2 FDA actions in our database.
Frequently Asked Questions
How often does HERON THERAPS INC have FDA actions?
HERON THERAPS INC 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 "NDA022445-14" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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