Package 43598-610-40

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 43598-610-40
Digits Only 4359861040
Product NDC 43598-610
Description

4 mL in 1 VIAL, GLASS (43598-610-40)

Marketing

Marketing Status
Marketed Since 2017-08-22
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": "948f7c4c-6a40-d240-3eb3-d9ae6e371429", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1860480", "1860485"], "spl_set_id": ["be3df07d-ea56-453a-25ad-c3cedc22712a"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 mL in 1 VIAL, GLASS (43598-610-40)", "package_ndc": "43598-610-40", "marketing_start_date": "20170822"}], "brand_name": "Docetaxel", "product_id": "43598-610_948f7c4c-6a40-d240-3eb3-d9ae6e371429", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "43598-610", "generic_name": "Docetaxel", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "80 mg/4mL"}], "application_number": "ANDA204193", "marketing_category": "ANDA", "marketing_start_date": "20170822", "listing_expiration_date": "20261231"}