Package 60505-0833-5

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-0833-5
Digits Only 6050508335
Product NDC 60505-0833
Description

1 BOTTLE, SPRAY in 1 CARTON (60505-0833-5) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2010-03-01
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": "6ace9d74-df2e-8b53-9bc8-72a794f3a21a", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["4f58c203-f649-a18e-aaf3-70b0797652f4"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (60505-0833-5)  / 200 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "60505-0833-5", "marketing_start_date": "20100301"}], "brand_name": "Azelastine Hydrochloride", "product_id": "60505-0833_6ace9d74-df2e-8b53-9bc8-72a794f3a21a", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "60505-0833", "generic_name": "azelastine hydrochloride", "labeler_name": "Apotex Corp.", "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"}