Package 85509-1057-4

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 85509-1057-4
Digits Only 8550910574
Product NDC 85509-1057
Product ID 85509-1057_4010608d-027c-0467-e063-6294a90a63e3
Description

12 TABLET, FILM COATED in 1 BOTTLE (85509-1057-4)

Marketing

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

Linked Drug Pages (1)

Ondansetron Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4010608d-027c-0467-e063-6294a90a63e3", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["40106070-6a25-5b0e-e063-6394a90a4197"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (85509-1057-4)", "package_ndc": "85509-1057-4", "marketing_start_date": "20250731"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "85509-1057_4010608d-027c-0467-e063-6294a90a63e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "85509-1057", "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"}