Package 10019-925-01

Brand: ifosfamide

Generic: ifosfamide
NDC Package

Package Facts

Identity

Package NDC 10019-925-01
Digits Only 1001992501
Product NDC 10019-925
Product ID 10019-925_7fd51853-2c9b-4291-85a8-a8ebf8782a92
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (10019-925-01) / 20 mL in 1 VIAL, SINGLE-DOSE (10019-925-82)

Marketing

Marketing Status
Marketed Since 1988-12-30
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": "7fd51853-2c9b-4291-85a8-a8ebf8782a92", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["UM20QQM95Y"], "rxcui": ["1791588", "1791593"], "spl_set_id": ["91e433a9-6800-43a6-ac13-a49a04a5aecd"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (10019-925-01)  / 20 mL in 1 VIAL, SINGLE-DOSE (10019-925-82)", "package_ndc": "10019-925-01", "marketing_start_date": "19881230"}], "brand_name": "IFOSFAMIDE", "product_id": "10019-925_7fd51853-2c9b-4291-85a8-a8ebf8782a92", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "10019-925", "generic_name": "IFOSFAMIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IFOSFAMIDE", "active_ingredients": [{"name": "IFOSFAMIDE", "strength": "1 g/20mL"}], "application_number": "NDA019763", "marketing_category": "NDA", "marketing_start_date": "19881230", "listing_expiration_date": "20261231"}