Package 0143-9551-10
Brand: daunorubicin hydrochloride
Generic: daunorubicin hydrochloridePackage Facts
Identity
Package NDC
0143-9551-10
Digits Only
0143955110
Product NDC
0143-9551
Description
10 VIAL in 1 BOX (0143-9551-10) / 4 mL in 1 VIAL (0143-9551-01)
Marketing
Marketing Status
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": "10 VIAL in 1 BOX (0143-9551-10) / 4 mL in 1 VIAL (0143-9551-01)", "package_ndc": "0143-9551-10", "marketing_start_date": "20180102"}], "brand_name": "Daunorubicin Hydrochloride", "product_id": "0143-9551_d77dc365-6db8-4bdc-81fc-7ac80bcc7699", "dosage_form": "INJECTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0143-9551", "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"}