Package 72485-210-08

Brand: busulfan

Generic: busulfan
NDC Package

Package Facts

Identity

Package NDC 72485-210-08
Digits Only 7248521008
Product NDC 72485-210
Product ID 72485-210_ae29e15b-df07-403f-8d07-f99e3ce501e7
Description

8 VIAL, SINGLE-DOSE in 1 CARTON (72485-210-08) / 10 mL in 1 VIAL, SINGLE-DOSE (72485-210-01)

Marketing

Marketing Status
Marketed Since 2019-06-01
Brand busulfan
Generic busulfan
Sample Package No

Linked Drug Pages (1)

Busulfan ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ae29e15b-df07-403f-8d07-f99e3ce501e7", "openfda": {"nui": ["N0000000236", "N0000175558"], "upc": ["0372485210015"], "unii": ["G1LN9045DK"], "rxcui": ["253113"], "spl_set_id": ["4049d57f-342e-4233-8292-fed6b8f128ec"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 VIAL, SINGLE-DOSE in 1 CARTON (72485-210-08)  / 10 mL in 1 VIAL, SINGLE-DOSE (72485-210-01)", "package_ndc": "72485-210-08", "marketing_start_date": "20190601"}], "brand_name": "Busulfan", "product_id": "72485-210_ae29e15b-df07-403f-8d07-f99e3ce501e7", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "72485-210", "generic_name": "Busulfan", "labeler_name": "Armas Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Busulfan", "active_ingredients": [{"name": "BUSULFAN", "strength": "6 mg/mL"}], "application_number": "ANDA210931", "marketing_category": "ANDA", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}