Package 71872-7107-1

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 71872-7107-1
Digits Only 7187271071
Product NDC 71872-7107
Description

1 VIAL, MULTI-DOSE in 1 BAG (71872-7107-1) / 20 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2018-05-30
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": "fc5e2428-7cc4-5cd3-e053-6394a90a7cd2", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504"], "spl_set_id": ["79756604-56e6-d0ef-e053-2991aa0adc99"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (71872-7107-1)  / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71872-7107-1", "marketing_start_date": "20180530"}], "brand_name": "Ondansetron", "product_id": "71872-7107_fc5e2428-7cc4-5cd3-e053-6394a90a7cd2", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "71872-7107", "generic_name": "Ondansetron", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA076781", "marketing_category": "ANDA", "marketing_start_date": "20061226", "listing_expiration_date": "20261231"}