Package 0143-9086-01

Brand: doxorubicin hydrochloride

Generic: doxorubicin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9086-01
Digits Only 0143908601
Product NDC 0143-9086
Description

1 VIAL in 1 BOX (0143-9086-01) / 25 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 1996-05-01
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": "77ae1280-f2df-49eb-bdcb-46dbd040ce46", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1191138", "1790097", "1790099", "1790100"], "spl_set_id": ["36924f82-6c05-4989-9f41-a398c0ad48e6"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9086-01)  / 25 mL in 1 VIAL", "package_ndc": "0143-9086-01", "marketing_start_date": "19960501"}], "brand_name": "Doxorubicin Hydrochloride", "product_id": "0143-9086_77ae1280-f2df-49eb-bdcb-46dbd040ce46", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0143-9086", "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"}