Package 65162-676-84

Brand: azelastine hydrochloride

Generic: azelastine
NDC Package

Package Facts

Identity

Package NDC 65162-676-84
Digits Only 6516267684
Product NDC 65162-676
Description

1 BOTTLE, SPRAY in 1 CARTON (65162-676-84) / 30 mL in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2017-09-05
Brand azelastine hydrochloride
Generic azelastine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "0ead3061-d60d-4911-91cc-489d3b5fe573", "openfda": {"upc": ["0365162676846"], "unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["7902605c-944a-4d7e-a7d4-eb4a71bcacdb"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (65162-676-84)  / 30 mL in 1 BOTTLE, SPRAY", "package_ndc": "65162-676-84", "marketing_start_date": "20170905"}], "brand_name": "Azelastine Hydrochloride", "product_id": "65162-676_0ead3061-d60d-4911-91cc-489d3b5fe573", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "65162-676", "generic_name": "Azelastine", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA204660", "marketing_category": "ANDA", "marketing_start_date": "20170905", "listing_expiration_date": "20261231"}