Package 0143-9531-01

Brand: ifosfamide

Generic: ifosfamide
NDC Package

Package Facts

Identity

Package NDC 0143-9531-01
Digits Only 0143953101
Product NDC 0143-9531
Description

1 VIAL in 1 BOX (0143-9531-01) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-06-10
Brand ifosfamide
Generic ifosfamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "dc31337c-ac3a-4d47-88d2-823e4181688a", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["UM20QQM95Y"], "rxcui": ["1791597", "1791599"], "spl_set_id": ["c90ab05f-8fe5-437e-a1c0-8b11ef63291e"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9531-01)  / 20 mL in 1 VIAL", "package_ndc": "0143-9531-01", "marketing_start_date": "20170610"}], "brand_name": "Ifosfamide", "product_id": "0143-9531_dc31337c-ac3a-4d47-88d2-823e4181688a", "dosage_form": "INJECTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "0143-9531", "generic_name": "Ifosfamide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ifosfamide", "active_ingredients": [{"name": "IFOSFAMIDE", "strength": "50 mg/mL"}], "application_number": "ANDA076619", "marketing_category": "ANDA", "marketing_start_date": "20170610", "listing_expiration_date": "20261231"}