Package 0409-7870-01

Brand: docetaxel

Generic: docetaxel anhydrous
NDC Package

Package Facts

Identity

Package NDC 0409-7870-01
Digits Only 0409787001
Product NDC 0409-7870
Description

1 VIAL, MULTI-DOSE in 1 CARTON (0409-7870-01) / 8 mL in 1 VIAL, MULTI-DOSE

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5b12d54f-e7fd-4369-afb3-431f6f08ec76", "openfda": {"nui": ["N0000175085", "N0000175592"], "unii": ["699121PHCA"], "rxcui": ["1093280"], "spl_set_id": ["644c5035-20d2-4686-beaa-bef08e99051c"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0409-7870-01)  / 8 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0409-7870-01", "marketing_start_date": "20210628"}], "brand_name": "Docetaxel", "product_id": "0409-7870_5b12d54f-e7fd-4369-afb3-431f6f08ec76", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "0409-7870", "generic_name": "DOCETAXEL ANHYDROUS", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL ANHYDROUS", "strength": "10 mg/mL"}], "application_number": "NDA022234", "marketing_category": "NDA", "marketing_start_date": "20210628", "listing_expiration_date": "20261231"}