United States · FDA National Drug Code directory
Azelastine Hydrochloride and Fluticasone Propionate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0480-2157_edea3e4b-7afc-4566-864d-acdf480a92af
- Product NDC
- 0480-2157
- Form
- SPRAY, METERED
- Composition / generic term
- Azelastine Hydrochloride and Fluticasone Propionate
- Labeler
- Teva Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250908
- Source listing expiry
- 20261231
Source-listed ingredients
- AZELASTINE HYDROCHLORIDE — 137 ug/1
- FLUTICASONE PROPIONATE — 50 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, SPRAY in 1 CARTON (0480-2157-57) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY · 0480-2157-57
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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