Package 0143-9550-01

Brand: daunorubicin hydrochloride

Generic: daunorubicin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9550-01
Digits Only 0143955001
Product NDC 0143-9550
Description

1 VIAL in 1 CARTON (0143-9550-01) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-01-02
Brand daunorubicin hydrochloride
Generic daunorubicin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d77dc365-6db8-4bdc-81fc-7ac80bcc7699", "openfda": {"unii": ["UD984I04LZ"], "rxcui": ["309650", "2002002"], "spl_set_id": ["227784a8-ce68-4dd4-8ac5-a65265969677"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0143-9550-01)  / 10 mL in 1 VIAL", "package_ndc": "0143-9550-01", "marketing_start_date": "20180102"}], "brand_name": "Daunorubicin Hydrochloride", "product_id": "0143-9550_d77dc365-6db8-4bdc-81fc-7ac80bcc7699", "dosage_form": "INJECTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0143-9550", "generic_name": "Daunorubicin Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Daunorubicin Hydrochloride", "active_ingredients": [{"name": "DAUNORUBICIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "NDA050731", "marketing_category": "NDA", "marketing_start_date": "20180102", "listing_expiration_date": "20261231"}