Package 0409-0302-01

Brand: topotecan

Generic: topotecan
NDC Package

Package Facts

Identity

Package NDC 0409-0302-01
Digits Only 0409030201
Product NDC 0409-0302
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0302-01) / 4 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2011-02-21
Brand topotecan
Generic topotecan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "293334d4-88f2-4ec2-9eed-20975ff65c0a", "openfda": {"unii": ["956S425ZCY"], "rxcui": ["1799424"], "spl_set_id": ["1d4e1cce-c57e-4a8b-be96-f95a2778e221"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0302-01)  / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-0302-01", "marketing_start_date": "20110221"}], "brand_name": "Topotecan", "product_id": "0409-0302_293334d4-88f2-4ec2-9eed-20975ff65c0a", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Topoisomerase Inhibitor [EPC]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0409-0302", "generic_name": "TOPOTECAN", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Topotecan", "active_ingredients": [{"name": "TOPOTECAN HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "NDA200582", "marketing_category": "NDA", "marketing_start_date": "20110221", "listing_expiration_date": "20261231"}