Package 25021-245-01

Brand: docetaxel

Generic: docetaxel anhydrous
NDC Package

Package Facts

Identity

Package NDC 25021-245-01
Digits Only 2502124501
Product NDC 25021-245
Product ID 25021-245_3897fe0d-2b9f-4be0-9076-9ccd693d4c86
Description

1 VIAL in 1 CARTON (25021-245-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-09-15
Brand docetaxel
Generic docetaxel anhydrous
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": "3897fe0d-2b9f-4be0-9076-9ccd693d4c86", "openfda": {"nui": ["N0000175085", "N0000175592"], "unii": ["699121PHCA"], "rxcui": ["1860480", "1860485"], "spl_set_id": ["30077f79-341f-4618-9ec5-23b17b212fae"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-245-01)  / 1 mL in 1 VIAL", "package_ndc": "25021-245-01", "marketing_start_date": "20170915"}, {"sample": false, "description": "1 VIAL in 1 CARTON (25021-245-04)  / 4 mL in 1 VIAL", "package_ndc": "25021-245-04", "marketing_start_date": "20170915"}], "brand_name": "Docetaxel", "product_id": "25021-245_3897fe0d-2b9f-4be0-9076-9ccd693d4c86", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "25021-245", "generic_name": "Docetaxel Anhydrous", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL ANHYDROUS", "strength": "20 mg/mL"}], "application_number": "ANDA207252", "marketing_category": "ANDA", "marketing_start_date": "20170915", "listing_expiration_date": "20261231"}