Package 63323-142-12

Brand: ifosfamide

Generic: ifosfamide
NDC Package

Package Facts

Identity

Package NDC 63323-142-12
Digits Only 6332314212
Product NDC 63323-142
Product ID 63323-142_14698d9d-9986-4f26-9bba-adb261002dc7
Description

1 VIAL, SINGLE-DOSE in 1 BOX (63323-142-12) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2003-01-28
Brand ifosfamide
Generic ifosfamide
Sample Package No

Linked Drug Pages (1)

Ifosfamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "14698d9d-9986-4f26-9bba-adb261002dc7", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["UM20QQM95Y"], "rxcui": ["1791593"], "spl_set_id": ["fb7f49af-ffe9-4969-a69c-8ed14dd0616b"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BOX (63323-142-12)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "63323-142-12", "marketing_start_date": "20030128"}], "brand_name": "Ifosfamide", "product_id": "63323-142_14698d9d-9986-4f26-9bba-adb261002dc7", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "63323-142", "generic_name": "IFOSFAMIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ifosfamide", "active_ingredients": [{"name": "IFOSFAMIDE", "strength": "1 g/1"}], "application_number": "ANDA076078", "marketing_category": "ANDA", "marketing_start_date": "20030128", "listing_expiration_date": "20261231"}