azelastine hydrochloride
Generic: azelastine hydrochloride
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
azelastine hydrochloride
Generic Name
azelastine hydrochloride
Labeler
proficient rx lp
Dosage Form
SPRAY, METERED
Routes
Active Ingredients
azelastine hydrochloride 137 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-449
Product ID
71205-449_91c72454-515f-4966-ad84-a78aba616fb5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077954
Listing Expiration
2026-12-31
Marketing Start
2010-03-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205449
Hyphenated Format
71205-449
Supplemental Identifiers
RxCUI
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
azelastine hydrochloride (source: ndc)
Generic Name
azelastine hydrochloride (source: ndc)
Application Number
ANDA077954 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 137 ug/1
Packaging
- 1 BOTTLE, SPRAY in 1 CARTON (71205-449-30) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "91c72454-515f-4966-ad84-a78aba616fb5", "openfda": {"upc": ["0371205449308"], "unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["11a74cae-a15b-4a6b-a8c0-1e6a234ee258"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (71205-449-30) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "71205-449-30", "marketing_start_date": "20200401"}], "brand_name": "Azelastine Hydrochloride", "product_id": "71205-449_91c72454-515f-4966-ad84-a78aba616fb5", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71205-449", "generic_name": "azelastine hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": "137 ug/1"}], "application_number": "ANDA077954", "marketing_category": "ANDA", "marketing_start_date": "20100301", "listing_expiration_date": "20261231"}