Package 0143-9205-01

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 0143-9205-01
Digits Only 0143920501
Product NDC 0143-9205
Product ID 0143-9205_5e524fd3-4dc2-4a16-b069-7790c57fcb72
Description

1 VIAL, GLASS in 1 CARTON (0143-9205-01) / 4 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2021-01-14
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": "5e524fd3-4dc2-4a16-b069-7790c57fcb72", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1860480", "1860485"], "spl_set_id": ["ff7fb2c2-97a7-4716-a269-925ca30cf0f1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (0143-9205-01)  / 4 mL in 1 VIAL, GLASS", "package_ndc": "0143-9205-01", "marketing_start_date": "20210114"}], "brand_name": "Docetaxel", "product_id": "0143-9205_5e524fd3-4dc2-4a16-b069-7790c57fcb72", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "0143-9205", "generic_name": "Docetaxel", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/mL"}], "application_number": "ANDA204490", "marketing_category": "ANDA", "marketing_start_date": "20210114", "listing_expiration_date": "20261231"}