Package 72485-215-04

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 72485-215-04
Digits Only 7248521504
Product NDC 72485-215
Product ID 72485-215_8c30c9d6-97ac-42b0-a5dc-97f56e94c3bb
Description

1 VIAL, SINGLE-USE in 1 CARTON (72485-215-04) / 4 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2020-01-15
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": "8c30c9d6-97ac-42b0-a5dc-97f56e94c3bb", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1860485"], "spl_set_id": ["7c1927a7-82ad-44ed-831e-5d4a88ac18f2"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (72485-215-04)  / 4 mL in 1 VIAL, SINGLE-USE", "package_ndc": "72485-215-04", "marketing_start_date": "20200115"}], "brand_name": "Docetaxel", "product_id": "72485-215_8c30c9d6-97ac-42b0-a5dc-97f56e94c3bb", "dosage_form": "INJECTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "72485-215", "generic_name": "Docetaxel", "labeler_name": "Armas Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "80 mg/4mL"}], "application_number": "ANDA210327", "marketing_category": "ANDA", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}