Package 45963-765-52

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 45963-765-52
Digits Only 4596376552
Product NDC 45963-765
Description

1 VIAL, GLASS in 1 CARTON (45963-765-52) / 4 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2014-09-01
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": "0bc8d3b7-f15e-4dbf-b51f-8baaa93b0e61", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1860480", "1860485"], "spl_set_id": ["2c806400-5fdc-4398-8475-37f700b3191f"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (45963-765-52)  / 4 mL in 1 VIAL, GLASS", "package_ndc": "45963-765-52", "marketing_start_date": "20140901"}], "brand_name": "Docetaxel", "product_id": "45963-765_0bc8d3b7-f15e-4dbf-b51f-8baaa93b0e61", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "45963-765", "generic_name": "Docetaxel", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/mL"}], "application_number": "NDA203551", "marketing_category": "NDA", "marketing_start_date": "20140901", "listing_expiration_date": "20261231"}