Package 67457-317-25

Brand: palonosetron hydrochloride

Generic: palonosetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67457-317-25
Digits Only 6745731725
Product NDC 67457-317
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (67457-317-25) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2018-09-20
Brand palonosetron hydrochloride
Generic palonosetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4fbe587d-ddb7-42fd-aad9-e749689d2276", "openfda": {"unii": ["23310D4I19"], "rxcui": ["1728055"], "spl_set_id": ["0a781796-bb74-4c5f-8d26-9ce520b818f7"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (67457-317-25)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67457-317-25", "marketing_start_date": "20180920"}], "brand_name": "Palonosetron Hydrochloride", "product_id": "67457-317_4fbe587d-ddb7-42fd-aad9-e749689d2276", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "67457-317", "generic_name": "Palonosetron Hydrochloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Palonosetron Hydrochloride", "active_ingredients": [{"name": "PALONOSETRON HYDROCHLORIDE", "strength": ".25 mg/5mL"}], "application_number": "ANDA206416", "marketing_category": "ANDA", "marketing_start_date": "20180920", "listing_expiration_date": "20261231"}