Package 42291-094-30

Brand: azelastine hydrochloride

Generic: azelastine
NDC Package

Package Facts

Identity

Package NDC 42291-094-30
Digits Only 4229109430
Product NDC 42291-094
Description

1 BOTTLE, SPRAY in 1 CARTON (42291-094-30) / 30 mL in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2021-03-03
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": "485b8c18-0782-37ea-e063-6394a90ad61e", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["bca75501-4140-4d77-e053-2a95a90a019f"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (42291-094-30)  / 30 mL in 1 BOTTLE, SPRAY", "package_ndc": "42291-094-30", "marketing_start_date": "20210303"}], "brand_name": "Azelastine Hydrochloride", "product_id": "42291-094_485b8c18-0782-37ea-e063-6394a90ad61e", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "42291-094", "generic_name": "Azelastine", "labeler_name": "AvKARE", "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": "20210303", "listing_expiration_date": "20271231"}