Package 47335-779-91

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 47335-779-91
Digits Only 4733577991
Product NDC 47335-779
Description

1 BOTTLE, SPRAY in 1 BOX (47335-779-91) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2012-05-24
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": "09652cb1-7315-4188-9f36-4e2b50fb764d", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["305c6dc8-8247-473d-9975-b02903af6d53"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 BOX (47335-779-91)  / 200 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "47335-779-91", "marketing_start_date": "20120524"}], "brand_name": "Azelastine Hydrochloride", "product_id": "47335-779_09652cb1-7315-4188-9f36-4e2b50fb764d", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "47335-779", "generic_name": "Azelastine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": "137 ug/1"}], "application_number": "ANDA090423", "marketing_category": "ANDA", "marketing_start_date": "20120524", "listing_expiration_date": "20261231"}