Package 71225-120-01

Brand: vivimusta

Generic: bendamustine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71225-120-01
Digits Only 7122512001
Product NDC 71225-120
Product ID 71225-120_c4b54079-dac2-4e01-a00f-6ceaa788f605
Description

1 VIAL, MULTI-DOSE in 1 CARTON (71225-120-01) / 4 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2022-12-07
Brand vivimusta
Generic bendamustine hydrochloride
Sample Package No

Linked Drug Pages (1)

VIVIMUSTA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c4b54079-dac2-4e01-a00f-6ceaa788f605", "openfda": {"unii": ["981Y8SX18M"], "rxcui": ["1726097", "2622914"], "spl_set_id": ["cbcc6eb7-aa62-4599-af49-05203fedb4bb"], "manufacturer_name": ["Slayback Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (71225-120-01)  / 4 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71225-120-01", "marketing_start_date": "20221207"}], "brand_name": "VIVIMUSTA", "product_id": "71225-120_c4b54079-dac2-4e01-a00f-6ceaa788f605", "dosage_form": "INJECTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "71225-120", "generic_name": "BENDAMUSTINE HYDROCHLORIDE", "labeler_name": "Slayback Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIVIMUSTA", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "NDA212209", "marketing_category": "NDA", "marketing_start_date": "20221207", "listing_expiration_date": "20261231"}