Package 46708-506-06

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 46708-506-06
Digits Only 4670850606
Product NDC 46708-506
Description

1 BOTTLE in 1 CARTON (46708-506-06) / 6 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-03-20
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": "753d7a69-b0da-4350-9dc5-97f26ebe5cc0", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["860805"], "spl_set_id": ["753d7a69-b0da-4350-9dc5-97f26ebe5cc0"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46708-506-06)  / 6 mL in 1 BOTTLE", "package_ndc": "46708-506-06", "marketing_start_date": "20190320"}], "brand_name": "AZELASTINE HYDROCHLORIDE", "product_id": "46708-506_753d7a69-b0da-4350-9dc5-97f26ebe5cc0", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "46708-506", "generic_name": "azelastine hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZELASTINE HYDROCHLORIDE", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA209620", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}