Package 72266-141-01

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72266-141-01
Digits Only 7226614101
Product NDC 72266-141
Description

1 BOTTLE, PLASTIC in 1 CARTON (72266-141-01) / 6 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2020-09-08
Brand azelastine hydrochloride
Generic azelastine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAOCULAR"], "spl_id": "3282899a-e3ac-971f-e063-6394a90ae53d", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["860805"], "spl_set_id": ["8ae2aec7-329b-41bf-89d5-f189afb782ee"], "manufacturer_name": ["Fosun Pharma USA Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72266-141-01)  / 6 mL in 1 BOTTLE, PLASTIC", "package_ndc": "72266-141-01", "marketing_start_date": "20200908"}], "brand_name": "Azelastine Hydrochloride", "product_id": "72266-141_3282899a-e3ac-971f-e063-6394a90ae53d", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72266-141", "generic_name": "Azelastine Hydrochloride", "labeler_name": "Fosun Pharma USA Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA210092", "marketing_category": "ANDA", "marketing_start_date": "20200908", "listing_expiration_date": "20261231"}