Package 72603-611-01

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-611-01
Digits Only 7260361101
Product NDC 72603-611
Description

1 BOTTLE, SPRAY in 1 CARTON (72603-611-01) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2025-07-01
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": "cb0aca6d-ff9c-4239-8681-d212a6764ba9", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["cb0aca6d-ff9c-4239-8681-d212a6764ba9"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (72603-611-01)  / 200 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "72603-611-01", "marketing_start_date": "20250701"}], "brand_name": "AZELASTINE HYDROCHLORIDE", "product_id": "72603-611_cb0aca6d-ff9c-4239-8681-d212a6764ba9", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72603-611", "generic_name": "AZELASTINE HYDROCHLORIDE", "labeler_name": "NorthStar Rx LLC", "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": "20250701", "listing_expiration_date": "20261231"}