Package 71205-449-30
Brand: azelastine hydrochloride
Generic: azelastine hydrochloridePackage Facts
Identity
Package NDC
71205-449-30
Digits Only
7120544930
Product NDC
71205-449
Description
1 BOTTLE, SPRAY in 1 CARTON (71205-449-30) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY
Marketing
Marketing Status
Brand
azelastine hydrochloride
Generic
azelastine hydrochloride
Sample Package
No
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"}