Package 72485-214-01

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 72485-214-01
Digits Only 7248521401
Product NDC 72485-214
Product ID 72485-214_029d2385-81d6-4bca-9472-c884d3fd7e24
Description

1 VIAL, SINGLE-USE in 1 CARTON (72485-214-01) / 1 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2020-01-15
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": "029d2385-81d6-4bca-9472-c884d3fd7e24", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1860480"], "spl_set_id": ["c00998dd-f859-435b-925b-4335299eaab3"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (72485-214-01)  / 1 mL in 1 VIAL, SINGLE-USE", "package_ndc": "72485-214-01", "marketing_start_date": "20200115"}], "brand_name": "Docetaxel", "product_id": "72485-214_029d2385-81d6-4bca-9472-c884d3fd7e24", "dosage_form": "INJECTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "72485-214", "generic_name": "Docetaxel", "labeler_name": "Armas Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/mL"}], "application_number": "ANDA210327", "marketing_category": "ANDA", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}