Package 55150-392-01

Brand: bendamustine hydrochloride

Generic: bendamustine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55150-392-01
Digits Only 5515039201
Product NDC 55150-392
Product ID 55150-392_4357b1f0-fcc2-448a-9580-13b55ba470de
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (55150-392-01) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-06-05
Brand bendamustine hydrochloride
Generic bendamustine hydrochloride
Sample Package No

Linked Drug Pages (1)

BENDAMUSTINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "4357b1f0-fcc2-448a-9580-13b55ba470de", "openfda": {"upc": ["0355150391011"], "unii": ["981Y8SX18M"], "rxcui": ["1805001", "1805007"], "spl_set_id": ["dbe34bc1-06b2-493f-8859-e8b143357aa8"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (55150-392-01)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-392-01", "marketing_start_date": "20230605"}], "brand_name": "BENDAMUSTINE HYDROCHLORIDE", "product_id": "55150-392_4357b1f0-fcc2-448a-9580-13b55ba470de", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "55150-392", "generic_name": "BENDAMUSTINE HYDROCHLORIDE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENDAMUSTINE HYDROCHLORIDE", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "100 mg/20mL"}], "application_number": "ANDA214739", "marketing_category": "ANDA", "marketing_start_date": "20230605", "listing_expiration_date": "20261231"}