Package 50090-7461-0

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7461-0
Digits Only 5009074610
Product NDC 50090-7461
Product ID 50090-7461_6f0629d0-5f20-406f-ad61-cf775f553772
Description

1 BOTTLE, SPRAY in 1 CARTON (50090-7461-0) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2024-11-19
Brand azelastine hydrochloride
Generic azelastine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "6f0629d0-5f20-406f-ad61-cf775f553772", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["fc9d031d-428d-4d53-8e63-feb96d5ab01a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (50090-7461-0)  / 200 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "50090-7461-0", "marketing_start_date": "20241119"}], "brand_name": "AZELASTINE HYDROCHLORIDE", "product_id": "50090-7461_6f0629d0-5f20-406f-ad61-cf775f553772", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-7461", "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": "ANDA212289", "marketing_category": "ANDA", "marketing_start_date": "20200508", "listing_expiration_date": "20261231"}