Package 51662-1377-1

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 51662-1377-1
Digits Only 5166213771
Product NDC 51662-1377
Description

20 mL in 1 VIAL (51662-1377-1)

Marketing

Marketing Status
Marketed Since 2020-05-21
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": "12504be9-9bd0-31db-e063-6394a90abc57", "openfda": {"upc": ["0363323374204"], "unii": ["NMH84OZK2B"], "rxcui": ["283504"], "spl_set_id": ["a62e2a6a-6235-7580-e053-2a95a90aa2b0"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL (51662-1377-1)", "package_ndc": "51662-1377-1", "marketing_start_date": "20200521"}], "brand_name": "ONDANSETRON", "product_id": "51662-1377_12504be9-9bd0-31db-e063-6394a90abc57", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "51662-1377", "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": "ANDA076974", "marketing_category": "ANDA", "marketing_start_date": "20200521", "listing_expiration_date": "20261231"}