Package 16729-251-05

Brand: bendamustine hydrochloride

Generic: bendamustine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16729-251-05
Digits Only 1672925105
Product NDC 16729-251
Product ID 16729-251_1d8759d2-4d4d-78ee-e063-6294a90a53ae
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (16729-251-05) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-12-07
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": "1d8759d2-4d4d-78ee-e063-6294a90a53ae", "openfda": {"upc": ["0316729251051"], "unii": ["981Y8SX18M"], "rxcui": ["1805001", "1805007"], "spl_set_id": ["33867f0f-f317-1fd0-e054-00144ff8d46c"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (16729-251-05)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "16729-251-05", "marketing_start_date": "20221207"}], "brand_name": "bendamustine hydrochloride", "product_id": "16729-251_1d8759d2-4d4d-78ee-e063-6294a90a53ae", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "16729-251", "generic_name": "bendamustine hydrochloride", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bendamustine hydrochloride", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "100 mg/20mL"}], "application_number": "ANDA205574", "marketing_category": "ANDA", "marketing_start_date": "20221207", "listing_expiration_date": "20261231"}