Package 63459-390-08

Brand: treanda

Generic: bendamustine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63459-390-08
Digits Only 6345939008
Product NDC 63459-390
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (63459-390-08) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2010-01-05
Brand treanda
Generic bendamustine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "77ae475d-2d59-4fe2-8de7-833b6fc9d51a", "openfda": {"unii": ["981Y8SX18M"], "rxcui": ["1805001", "1805004", "1805007", "1805009", "1805011", "1805012", "1805015", "1805016"], "spl_set_id": ["39d53698-57fa-7c99-fc5b-f52a55684826"], "manufacturer_name": ["Cephalon, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (63459-390-08)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63459-390-08", "marketing_start_date": "20100105"}], "brand_name": "TREANDA", "product_id": "63459-390_77ae475d-2d59-4fe2-8de7-833b6fc9d51a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "63459-390", "generic_name": "Bendamustine Hydrochloride", "labeler_name": "Cephalon, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TREANDA", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "25 mg/5mL"}], "application_number": "NDA022249", "marketing_category": "NDA", "marketing_start_date": "20100105", "listing_expiration_date": "20261231"}