Package 0409-4235-01

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 0409-4235-01
Digits Only 0409423501
Product NDC 0409-4235
Product ID 0409-4235_0eff97af-e2cd-46d7-84d3-0445a0910b1a
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (0409-4235-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2021-06-28
Brand docetaxel
Generic docetaxel
Sample Package No

Linked Drug Pages (1)

Docetaxel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0eff97af-e2cd-46d7-84d3-0445a0910b1a", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1001405", "1860480"], "spl_set_id": ["6b9999bb-869e-4d25-838c-23c3ab280044"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-4235-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-4235-01", "marketing_start_date": "20210628"}], "brand_name": "Docetaxel", "product_id": "0409-4235_0eff97af-e2cd-46d7-84d3-0445a0910b1a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "0409-4235", "generic_name": "DOCETAXEL", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/mL"}], "application_number": "NDA022234", "marketing_category": "NDA", "marketing_start_date": "20210628", "listing_expiration_date": "20261231"}