Package 68788-4056-2

Brand: azelastine hydrochloride

Generic: azelastine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-4056-2
Digits Only 6878840562
Product NDC 68788-4056
Description

1 BOTTLE, SPRAY in 1 CARTON (68788-4056-2) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2025-11-17
Brand azelastine hydrochloride
Generic azelastine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "a2ba9c1d-b21f-4816-bbe6-949a49e38572", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["1797867"], "spl_set_id": ["a2ba9c1d-b21f-4816-bbe6-949a49e38572"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (68788-4056-2)  / 200 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "68788-4056-2", "marketing_start_date": "20251117"}], "brand_name": "Azelastine Hydrochloride", "product_id": "68788-4056_a2ba9c1d-b21f-4816-bbe6-949a49e38572", "dosage_form": "SPRAY, METERED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68788-4056", "generic_name": "azelastine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": "137 ug/1"}], "application_number": "ANDA077954", "marketing_category": "ANDA", "marketing_start_date": "20251117", "listing_expiration_date": "20261231"}