Package 10019-079-01

Brand: bendamustine hydrochloride

Generic: bendamustine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10019-079-01
Digits Only 1001907901
Product NDC 10019-079
Product ID 10019-079_3d05da71-982b-4d45-8d2f-4eee390f5172
Description

1 VIAL, MULTI-DOSE in 1 CARTON (10019-079-01) / 1 INJECTION in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2022-12-15
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": "3d05da71-982b-4d45-8d2f-4eee390f5172", "openfda": {"unii": ["981Y8SX18M"], "rxcui": ["1726097"], "spl_set_id": ["766b73e2-49bb-47f9-bbb1-44cfa1a3197e"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (10019-079-01)  / 1 INJECTION in 1 VIAL, MULTI-DOSE", "package_ndc": "10019-079-01", "marketing_start_date": "20221215"}], "brand_name": "BENDAMUSTINE HYDROCHLORIDE", "product_id": "10019-079_3d05da71-982b-4d45-8d2f-4eee390f5172", "dosage_form": "INJECTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "10019-079", "generic_name": "bendamustine hydrochloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENDAMUSTINE HYDROCHLORIDE", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "NDA216078", "marketing_category": "NDA", "marketing_start_date": "20221215", "listing_expiration_date": "20261231"}