Package 71288-144-08

Brand: docetaxel anhydrous

Generic: docetaxel anhydrous
NDC Package

Package Facts

Identity

Package NDC 71288-144-08
Digits Only 7128814408
Product NDC 71288-144
Description

1 VIAL, MULTI-DOSE in 1 CARTON (71288-144-08) / 8 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2018-08-24
Brand docetaxel anhydrous
Generic docetaxel anhydrous
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "77b41d41-9975-428a-865a-1593d21b3d99", "openfda": {"nui": ["N0000175085", "N0000175592"], "unii": ["699121PHCA"], "rxcui": ["1093280"], "spl_set_id": ["9fb533da-a7ba-4c2b-8e4f-8e336ba55d12"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (71288-144-08)  / 8 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71288-144-08", "marketing_start_date": "20180824"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (71288-144-16)  / 16 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71288-144-16", "marketing_start_date": "20180824"}], "brand_name": "Docetaxel anhydrous", "product_id": "71288-144_77b41d41-9975-428a-865a-1593d21b3d99", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "71288-144", "generic_name": "Docetaxel anhydrous", "labeler_name": "Meitheal Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel anhydrous", "active_ingredients": [{"name": "DOCETAXEL ANHYDROUS", "strength": "10 mg/mL"}], "application_number": "ANDA209634", "marketing_category": "ANDA", "marketing_start_date": "20180824", "listing_expiration_date": "20261231"}