Package 0338-3991-01
Brand: ifex
Generic: ifosfamidePackage Facts
Identity
Package NDC
0338-3991-01
Digits Only
0338399101
Product NDC
0338-3991
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (0338-3991-01) / 20 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
ifex
Generic
ifosfamide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fdee89dd-171b-4c31-9651-919cd8aaff39", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["UM20QQM95Y"], "rxcui": ["1791588", "1791591", "1791593", "1791595"], "spl_set_id": ["b7241707-7538-4d1a-91e7-3a25a91e0b9a"], "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 (0338-3991-01) / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0338-3991-01", "marketing_start_date": "19881230"}], "brand_name": "IFEX", "product_id": "0338-3991_fdee89dd-171b-4c31-9651-919cd8aaff39", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "0338-3991", "generic_name": "ifosfamide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IFEX", "active_ingredients": [{"name": "IFOSFAMIDE", "strength": "1 g/20mL"}], "application_number": "NDA019763", "marketing_category": "NDA", "marketing_start_date": "19881230", "listing_expiration_date": "20261231"}