Package 67457-781-08

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 67457-781-08
Digits Only 6745778108
Product NDC 67457-781
Description

1 VIAL, MULTI-DOSE in 1 CARTON (67457-781-08) / 8 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2019-06-18
Brand docetaxel
Generic docetaxel
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fea50522-6e4c-4ae0-81ac-53863693cc06", "openfda": {"upc": ["0367457781082"], "unii": ["15H5577CQD"], "rxcui": ["1001405"], "spl_set_id": ["a6417655-9448-4886-ba03-f57f36bcbd14"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (67457-781-08)  / 8 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "67457-781-08", "marketing_start_date": "20190618"}], "brand_name": "Docetaxel", "product_id": "67457-781_fea50522-6e4c-4ae0-81ac-53863693cc06", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "67457-781", "generic_name": "Docetaxel", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/mL"}], "application_number": "ANDA208137", "marketing_category": "ANDA", "marketing_start_date": "20190618", "listing_expiration_date": "20261231"}