Package 50090-2330-0

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-2330-0
Digits Only 5009023300
Product NDC 50090-2330
Description

1 BOTTLE, SPRAY in 1 CARTON (50090-2330-0) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2016-03-15
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": "d2dfdb55-40a8-441e-8454-9f3b1eb3e89d", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["02257284-4bb1-4fe6-8134-e5a67a645114"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (50090-2330-0)  / 200 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "50090-2330-0", "marketing_start_date": "20160315"}], "brand_name": "Azelastine Hydrochloride", "product_id": "50090-2330_d2dfdb55-40a8-441e-8454-9f3b1eb3e89d", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-2330", "generic_name": "azelastine hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}