Package 51817-170-01

Brand: busulfan

Generic: busulfan
NDC Package

Package Facts

Identity

Package NDC 51817-170-01
Digits Only 5181717001
Product NDC 51817-170
Description

8 VIAL in 1 PACKAGE (51817-170-01) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-05-19
Brand busulfan
Generic busulfan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "df501797-3c7e-5ae2-e053-2995a90a99e8", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["G1LN9045DK"], "rxcui": ["253113"], "spl_set_id": ["d0fe44f9-7747-4909-b927-3b24aa6e7e09"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Pharmascience Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 VIAL in 1 PACKAGE (51817-170-01)  / 10 mL in 1 VIAL", "package_ndc": "51817-170-01", "marketing_start_date": "20170519"}], "brand_name": "Busulfan", "product_id": "51817-170_df501797-3c7e-5ae2-e053-2995a90a99e8", "dosage_form": "INJECTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "51817-170", "generic_name": "busulfan", "labeler_name": "Pharmascience Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Busulfan", "active_ingredients": [{"name": "BUSULFAN", "strength": "6 mg/mL"}], "application_number": "ANDA207050", "marketing_category": "ANDA", "marketing_start_date": "20170519", "listing_expiration_date": "20261231"}