Package 25021-254-16

Brand: docetaxel

Generic: docetaxel anhydrous
NDC Package

Package Facts

Identity

Package NDC 25021-254-16
Digits Only 2502125416
Product NDC 25021-254
Product ID 25021-254_841e3024-e160-4c4b-93d3-1e79d628d95b
Description

1 VIAL in 1 CARTON (25021-254-16) / 16 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-08-01
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": "841e3024-e160-4c4b-93d3-1e79d628d95b", "openfda": {"nui": ["N0000175085", "N0000175592"], "unii": ["699121PHCA"], "rxcui": ["1093280"], "spl_set_id": ["6b227144-c844-4549-960c-cc3ac5c13b2b"], "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 (25021-254-08)  / 8 mL in 1 VIAL", "package_ndc": "25021-254-08", "marketing_start_date": "20230801"}, {"sample": false, "description": "1 VIAL in 1 CARTON (25021-254-16)  / 16 mL in 1 VIAL", "package_ndc": "25021-254-16", "marketing_start_date": "20230801"}], "brand_name": "Docetaxel", "product_id": "25021-254_841e3024-e160-4c4b-93d3-1e79d628d95b", "dosage_form": "INJECTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "25021-254", "generic_name": "Docetaxel Anhydrous", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL ANHYDROUS", "strength": "10 mg/mL"}], "application_number": "ANDA213510", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}