Package 85509-1075-4

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 85509-1075-4
Digits Only 8550910754
Product NDC 85509-1075
Description

12 TABLET, FILM COATED in 1 BOTTLE (85509-1075-4)

Marketing

Marketing Status
Marketed Since 2025-07-31
Brand ondansetron hydrochloride
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f67d4c3-6148-4973-e063-6294a90aa5df", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["3a79fc2b-9ea3-a808-e063-6394a90ae794"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (85509-1075-1)", "package_ndc": "85509-1075-1", "marketing_start_date": "20250731"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (85509-1075-2)", "package_ndc": "85509-1075-2", "marketing_start_date": "20250731"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85509-1075-3)", "package_ndc": "85509-1075-3", "marketing_start_date": "20250731"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (85509-1075-4)", "package_ndc": "85509-1075-4", "marketing_start_date": "20250731"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (85509-1075-5)", "package_ndc": "85509-1075-5", "marketing_start_date": "20250731"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85509-1075-6)", "package_ndc": "85509-1075-6", "marketing_start_date": "20250731"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "85509-1075_3f67d4c3-6148-4973-e063-6294a90aa5df", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "85509-1075", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}