Package 67877-477-50

Brand: azelastine

Generic: azelastine
NDC Package

Package Facts

Identity

Package NDC 67877-477-50
Digits Only 6787747750
Product NDC 67877-477
Product ID 67877-477_25fdc0b5-0653-4aed-b3a4-cfbfad9f12ae
Description

1 SPRAY, METERED in 1 BOTTLE (67877-477-50)

Marketing

Marketing Status
Marketed Since 2017-08-18
Brand azelastine
Generic azelastine
Sample Package No

Linked Drug Pages (1)

Azelastine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "25fdc0b5-0653-4aed-b3a4-cfbfad9f12ae", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["77b20c6b-f30f-42a9-a0ef-d5d0bd3feb56"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SPRAY, METERED in 1 BOTTLE (67877-477-50)", "package_ndc": "67877-477-50", "marketing_start_date": "20170818"}], "brand_name": "Azelastine", "product_id": "67877-477_25fdc0b5-0653-4aed-b3a4-cfbfad9f12ae", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67877-477", "generic_name": "Azelastine", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": "137 ug/1"}], "application_number": "ANDA208156", "marketing_category": "ANDA", "marketing_start_date": "20170818", "listing_expiration_date": "20261231"}