Package 0409-4759-01

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 0409-4759-01
Digits Only 0409475901
Product NDC 0409-4759
Description

1 VIAL, MULTI-DOSE in 1 CARTON (0409-4759-01) / 20 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2006-11-07
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "f4d4b538-f4fd-49d7-ac02-b72d48c52e59", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["6a11f61b-2318-4382-2b91-4366e4bb53fa"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0409-4759-01)  / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0409-4759-01", "marketing_start_date": "20061107"}], "brand_name": "Ondansetron", "product_id": "0409-4759_f4d4b538-f4fd-49d7-ac02-b72d48c52e59", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0409-4759", "generic_name": "ONDANSETRON", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA077473", "marketing_category": "ANDA", "marketing_start_date": "20061107", "listing_expiration_date": "20261231"}