Package 0143-9248-01

Brand: dexrazoxane

Generic: dexrazoxane
NDC Package

Package Facts

Identity

Package NDC 0143-9248-01
Digits Only 0143924801
Product NDC 0143-9248
Product ID 0143-9248_032583c8-f4e7-4105-b92e-b5c3f96ca80e
Description

1 VIAL in 1 BOX (0143-9248-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-10-05
Brand dexrazoxane
Generic dexrazoxane
Sample Package No

Linked Drug Pages (1)

Dexrazoxane ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "032583c8-f4e7-4105-b92e-b5c3f96ca80e", "openfda": {"unii": ["5346058Q7S"], "rxcui": ["1736585", "1736590"], "spl_set_id": ["68089182-d4a2-4053-8d0d-fc97a901515d"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9248-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9248-01", "marketing_start_date": "20171005"}], "brand_name": "Dexrazoxane", "product_id": "0143-9248_032583c8-f4e7-4105-b92e-b5c3f96ca80e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "0143-9248", "generic_name": "Dexrazoxane", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexrazoxane", "active_ingredients": [{"name": "DEXRAZOXANE HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076068", "marketing_category": "ANDA", "marketing_start_date": "20050331", "listing_expiration_date": "20261231"}