Package 0143-9088-01

Brand: doxorubicin hydrochloride

Generic: doxorubicin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9088-01
Digits Only 0143908801
Product NDC 0143-9088
Description

1 VIAL in 1 BOX (0143-9088-01) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2019-10-01
Brand doxorubicin hydrochloride
Generic doxorubicin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "7c916380-3ae0-4a64-945d-7b0da46b9715", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1191138", "1790097", "1790099", "1790100"], "spl_set_id": ["971de64b-ff09-4370-afd9-6eb1093ad27d"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9088-01)  / 5 mL in 1 VIAL", "package_ndc": "0143-9088-01", "marketing_start_date": "20191001"}], "brand_name": "Doxorubicin Hydrochloride", "product_id": "0143-9088_7c916380-3ae0-4a64-945d-7b0da46b9715", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0143-9088", "generic_name": "Doxorubicin Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxorubicin Hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA062975", "marketing_category": "ANDA", "marketing_start_date": "19960501", "listing_expiration_date": "20261231"}