Package 60505-6439-1
Brand: palonosetron
Generic: palonosetron hydrochloridePackage Facts
Identity
Package NDC
60505-6439-1
Digits Only
6050564391
Product NDC
60505-6439
Description
1 VIAL in 1 CARTON (60505-6439-1) / 5 mL in 1 VIAL
Marketing
Marketing Status
Brand
palonosetron
Generic
palonosetron hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "77da1c6e-4a91-4042-a227-57904bbe2f07", "openfda": {"upc": ["0360505643912"], "unii": ["23310D4I19"], "rxcui": ["1728055"], "spl_set_id": ["4af600d1-0ab1-41c5-af2f-9dc24cf3c90e"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (60505-6439-1) / 5 mL in 1 VIAL", "package_ndc": "60505-6439-1", "marketing_start_date": "20251031"}], "brand_name": "Palonosetron", "product_id": "60505-6439_77da1c6e-4a91-4042-a227-57904bbe2f07", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "60505-6439", "generic_name": "Palonosetron Hydrochloride", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Palonosetron", "active_ingredients": [{"name": "PALONOSETRON HYDROCHLORIDE", "strength": ".25 mg/5mL"}], "application_number": "ANDA205648", "marketing_category": "ANDA", "marketing_start_date": "20251024", "listing_expiration_date": "20261231"}