Package 25021-783-05
Brand: palonosetron hydrochloride
Generic: palonosetron hydrochloridePackage Facts
Identity
Package NDC
25021-783-05
Digits Only
2502178305
Product NDC
25021-783
Description
1 VIAL in 1 CARTON (25021-783-05) / 5 mL in 1 VIAL
Marketing
Marketing Status
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": "5679dbc2-6417-4a54-a627-7f72293879ad", "openfda": {"unii": ["23310D4I19"], "rxcui": ["1728055"], "spl_set_id": ["6e60d03d-eae6-4924-a507-e77ea077c1ab"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-783-05) / 5 mL in 1 VIAL", "package_ndc": "25021-783-05", "marketing_start_date": "20180615"}], "brand_name": "palonosetron hydrochloride", "product_id": "25021-783_5679dbc2-6417-4a54-a627-7f72293879ad", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "25021-783", "generic_name": "palonosetron hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "palonosetron hydrochloride", "active_ingredients": [{"name": "PALONOSETRON HYDROCHLORIDE", "strength": ".05 mg/mL"}], "application_number": "ANDA204289", "marketing_category": "ANDA", "marketing_start_date": "20180615", "listing_expiration_date": "20261231"}