ESTRASORB
Summary
FDA approved ESTRASORB by EXELTIS USA INC. NDA (New Drug) approval (Labeling) on 2024-09-10. EMULSION, TOPICAL.
Details
Source
Drug Approval
External ID
NDA021371-9
Action Date
2024-09-10
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ESTRASORB, EMULSION, TOPICAL. Application: NDA021371
Company
Context & Analysis
EXELTIS USA INC has 2 FDA actions in our database.
Frequently Asked Questions
How often does EXELTIS USA INC have FDA actions?
EXELTIS USA 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 "NDA021371-9" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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