Package 0404-9930-02

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 0404-9930-02
Digits Only 0404993002
Product NDC 0404-9930
Description

1 VIAL, SINGLE-USE in 1 BAG (0404-9930-02) / 2 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2022-01-13
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": "87fe0041-54b9-4cef-83b1-41f7d0d9232d", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["1a44601b-c31c-4779-a688-28cc4cc75e8b"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 BAG (0404-9930-02)  / 2 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0404-9930-02", "marketing_start_date": "20220113"}], "brand_name": "ONDANSETRON", "product_id": "0404-9930_87fe0041-54b9-4cef-83b1-41f7d0d9232d", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0404-9930", "generic_name": "ONDANSETRON", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA203711", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}