FLUTICASONE PROPIONATE ALLERGY RELIEF (FLUTICASONE PROPIONATE)
Summary
FDA approved FLUTICASONE PROPIONATE ALLERGY RELIEF (FLUTICASONE PROPIONATE) by GLENMARK SPECLT. ANDA (Generic) approval on 2026-03-16. SPRAY, METERED, NASAL.
Details
Source
Drug Approval
External ID
ANDA218742-1
Action Date
2026-03-16
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
FLUTICASONE PROPIONATE ALLERGY RELIEF (generic: FLUTICASONE PROPIONATE), SPRAY, METERED, NASAL. Application: ANDA218742
Company
Context & Analysis
GLENMARK SPECLT has 8 FDA actions in our database.
Frequently Asked Questions
How often does GLENMARK SPECLT have FDA actions?
GLENMARK SPECLT has 8 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 "ANDA218742-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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