Package 70069-091-01
Brand: azelastine hydrochloride
Generic: azelastine hydrochloridePackage Facts
Identity
Package NDC
70069-091-01
Digits Only
7006909101
Product NDC
70069-091
Description
1 BOTTLE in 1 CARTON (70069-091-01) / 6 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
azelastine hydrochloride
Generic
azelastine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "9d82b566-97da-4162-a649-b44f3e516d9a", "openfda": {"upc": ["0370069091012"], "unii": ["0L591QR10I"], "rxcui": ["860805"], "spl_set_id": ["72406ded-7886-41fb-b5c8-2d27a149aa34"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70069-091-01) / 6 mL in 1 BOTTLE", "package_ndc": "70069-091-01", "marketing_start_date": "20190408"}], "brand_name": "Azelastine Hydrochloride", "product_id": "70069-091_9d82b566-97da-4162-a649-b44f3e516d9a", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70069-091", "generic_name": "Azelastine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA207411", "marketing_category": "ANDA", "marketing_start_date": "20190408", "listing_expiration_date": "20261231"}