Package 67184-0507-5

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 67184-0507-5
Digits Only 6718405075
Product NDC 67184-0507
Description

5 VIAL, SINGLE-USE in 1 CARTON (67184-0507-5) / 2 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2014-09-08
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": "cd294344-e9fc-4b11-811f-0a8843db3227", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["5e09e262-dadf-4ae0-825e-448ea8dac174"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, SINGLE-USE in 1 CARTON (67184-0507-5)  / 2 mL in 1 VIAL, SINGLE-USE", "package_ndc": "67184-0507-5", "marketing_start_date": "20140908"}], "brand_name": "ONDANSETRON", "product_id": "67184-0507_cd294344-e9fc-4b11-811f-0a8843db3227", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "67184-0507", "generic_name": "ONDANSETRON", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "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": "20140908", "listing_expiration_date": "20261231"}