Package 71288-152-04

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 71288-152-04
Digits Only 7128815204
Product NDC 71288-152
Product ID 71288-152_bf235693-ce1a-4f89-b33a-8aaf93efb275
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-152-04) / 4 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-05-13
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": "bf235693-ce1a-4f89-b33a-8aaf93efb275", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1860480", "1860485"], "spl_set_id": ["f970e352-3d43-4cc4-a859-503ec37b6e22"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-152-04)  / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-152-04", "marketing_start_date": "20250513"}], "brand_name": "Docetaxel", "product_id": "71288-152_bf235693-ce1a-4f89-b33a-8aaf93efb275", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "71288-152", "generic_name": "Docetaxel", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/mL"}], "application_number": "ANDA213768", "marketing_category": "ANDA", "marketing_start_date": "20250513", "listing_expiration_date": "20261231"}