Package 71288-409-05

Brand: palonosetron hydrochloride

Generic: palonosetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71288-409-05
Digits Only 7128840905
Product NDC 71288-409
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-409-05) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-08-14
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": "a1f0c351-fcb5-4d19-94b1-3317b70be391", "openfda": {"unii": ["23310D4I19"], "rxcui": ["1728055"], "spl_set_id": ["11bb07b2-6530-45ab-a916-ba9dd3107fc3"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-409-05)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-409-05", "marketing_start_date": "20230814"}], "brand_name": "Palonosetron Hydrochloride", "product_id": "71288-409_a1f0c351-fcb5-4d19-94b1-3317b70be391", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "71288-409", "generic_name": "Palonosetron Hydrochloride", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Palonosetron Hydrochloride", "active_ingredients": [{"name": "PALONOSETRON HYDROCHLORIDE", "strength": ".25 mg/5mL"}], "application_number": "ANDA215861", "marketing_category": "ANDA", "marketing_start_date": "20230814", "listing_expiration_date": "20261231"}