Package 72266-235-01

Brand: dexrazoxane

Generic: dexrazoxane for injection
NDC Package

Package Facts

Identity

Package NDC 72266-235-01
Digits Only 7226623501
Product NDC 72266-235
Description

1 VIAL in 1 CARTON (72266-235-01) / 25 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-11-01
Brand dexrazoxane
Generic dexrazoxane for injection
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "39134f54-58a4-ca41-e063-6394a90ac300", "openfda": {"upc": ["0372266101013", "0372266235015"], "unii": ["5346058Q7S"], "rxcui": ["1736585", "1736590"], "spl_set_id": ["c1d98fbe-5fd9-4518-b1a5-fac92e32928f"], "manufacturer_name": ["Fosun Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (72266-235-01)  / 25 mL in 1 VIAL", "package_ndc": "72266-235-01", "marketing_start_date": "20211101"}], "brand_name": "Dexrazoxane", "product_id": "72266-235_39134f54-58a4-ca41-e063-6394a90ac300", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "72266-235", "generic_name": "Dexrazoxane for Injection", "labeler_name": "Fosun Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexrazoxane", "active_ingredients": [{"name": "DEXRAZOXANE HYDROCHLORIDE", "strength": "250 mg/25mL"}], "application_number": "ANDA207321", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}