Package 72611-716-72

Brand: dexrazoxane

Generic: dexrazoxane for injection
NDC Package

Package Facts

Identity

Package NDC 72611-716-72
Digits Only 7261171672
Product NDC 72611-716
Product ID 72611-716_04d9a64e-d4e5-22d2-bfef-32594ee380d2
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (72611-716-72) / 50 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-06-01
Brand dexrazoxane
Generic dexrazoxane for injection
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": "04d9a64e-d4e5-22d2-bfef-32594ee380d2", "openfda": {"unii": ["5346058Q7S"], "rxcui": ["1736590"], "spl_set_id": ["9cbd2987-10bb-eceb-153d-ee7be1ed0c84"], "manufacturer_name": ["Almaject, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72611-716-72)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72611-716-72", "marketing_start_date": "20220601"}], "brand_name": "Dexrazoxane", "product_id": "72611-716_04d9a64e-d4e5-22d2-bfef-32594ee380d2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "72611-716", "generic_name": "Dexrazoxane for Injection", "labeler_name": "Almaject, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexrazoxane", "active_ingredients": [{"name": "DEXRAZOXANE HYDROCHLORIDE", "strength": "500 mg/50mL"}], "application_number": "ANDA207321", "marketing_category": "ANDA", "marketing_start_date": "20220601", "listing_expiration_date": "20261231"}