Package 51662-1366-1

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 51662-1366-1
Digits Only 5166213661
Product NDC 51662-1366
Description

2 mL in 1 VIAL (51662-1366-1)

Marketing

Marketing Status
Marketed Since 2019-12-08
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": "ef7bd6e6-d630-7e93-e053-2a95a90aef83", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["993cd1d7-70a1-a431-e053-2a95a90a5771"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL (51662-1366-1)", "package_ndc": "51662-1366-1", "marketing_start_date": "20191208"}], "brand_name": "ONDANSETRON", "product_id": "51662-1366_ef7bd6e6-d630-7e93-e053-2a95a90aef83", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "51662-1366", "generic_name": "ONDANSETRON", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA076972", "marketing_category": "ANDA", "marketing_start_date": "20191208", "listing_expiration_date": "20261231"}