Strength
137 ug/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
47335077991
Classification
Generic
Dosage Form
SPRAY, METERED
Route
NASAL
Last Updated
2/18/2026
Active Ingredients
AZELASTINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA090423On Market Since
5/24/2012
Pharmacological Classes
Histamine H1 Receptor Antagonists
Histamine-1 Receptor Antagonist
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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