Package 60505-6228-0

Brand: bendamustine hydrochloride

Generic: bendamustine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-6228-0
Digits Only 6050562280
Product NDC 60505-6228
Product ID 60505-6228_5ebe4a1f-c7d6-95a3-8f21-8deebf9bd43a
Description

1 VIAL, MULTI-DOSE in 1 CARTON (60505-6228-0) / 5 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2023-04-26
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": "5ebe4a1f-c7d6-95a3-8f21-8deebf9bd43a", "openfda": {"unii": ["981Y8SX18M"], "rxcui": ["1726097"], "spl_set_id": ["085dd54c-4212-d879-afef-ee52732a48c0"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (60505-6228-0)  / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "60505-6228-0", "marketing_start_date": "20230426"}], "brand_name": "Bendamustine Hydrochloride", "product_id": "60505-6228_5ebe4a1f-c7d6-95a3-8f21-8deebf9bd43a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "60505-6228", "generic_name": "Bendamustine Hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bendamustine Hydrochloride", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "NDA215033", "marketing_category": "NDA", "marketing_start_date": "20230426", "listing_expiration_date": "20261231"}