Package 72485-216-08

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 72485-216-08
Digits Only 7248521608
Product NDC 72485-216
Product ID 72485-216_10308491-d534-4e9f-9fcc-8d8a3eda213d
Description

1 VIAL, SINGLE-USE in 1 CARTON (72485-216-08) / 8 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": "10308491-d534-4e9f-9fcc-8d8a3eda213d", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1861411"], "spl_set_id": ["0dd863ec-f9dc-456c-9df5-4e9210d6cbb0"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (72485-216-08)  / 8 mL in 1 VIAL, SINGLE-USE", "package_ndc": "72485-216-08", "marketing_start_date": "20200115"}], "brand_name": "Docetaxel", "product_id": "72485-216_10308491-d534-4e9f-9fcc-8d8a3eda213d", "dosage_form": "INJECTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "72485-216", "generic_name": "Docetaxel", "labeler_name": "Armas Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "160 mg/8mL"}], "application_number": "ANDA210327", "marketing_category": "ANDA", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}