Package 0409-0366-01

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 0409-0366-01
Digits Only 0409036601
Product NDC 0409-0366
Product ID 0409-0366_297f1202-b539-41ee-bf52-4b9b04dd3a60
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0366-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2016-08-24
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": "297f1202-b539-41ee-bf52-4b9b04dd3a60", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1001405", "1860480"], "spl_set_id": ["3104aab1-cd6e-4ad2-8e0a-286a0c5d1940"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0366-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-0366-01", "marketing_start_date": "20160824"}], "brand_name": "Docetaxel", "product_id": "0409-0366_297f1202-b539-41ee-bf52-4b9b04dd3a60", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "0409-0366", "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": "20160824", "listing_expiration_date": "20261231"}