Package 72205-248-01

Brand: dexrazoxane

Generic: dexrazoxane
NDC Package

Package Facts

Identity

Package NDC 72205-248-01
Digits Only 7220524801
Product NDC 72205-248
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (72205-248-01) / 50 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-04-09
Brand dexrazoxane
Generic dexrazoxane
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "bdcb7617-046b-4db9-94ba-b10102565868", "openfda": {"upc": ["0372205248014", "0372205247017"], "unii": ["5346058Q7S"], "rxcui": ["1736585", "1736590"], "spl_set_id": ["a7c01089-85f5-40aa-b679-f53a425b4d68"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72205-248-01)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72205-248-01", "marketing_start_date": "20250409"}], "brand_name": "Dexrazoxane", "product_id": "72205-248_bdcb7617-046b-4db9-94ba-b10102565868", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "72205-248", "generic_name": "Dexrazoxane", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexrazoxane", "active_ingredients": [{"name": "DEXRAZOXANE HYDROCHLORIDE", "strength": "500 mg/50mL"}], "application_number": "ANDA216748", "marketing_category": "ANDA", "marketing_start_date": "20250326", "listing_expiration_date": "20261231"}