Package 71288-102-10

Brand: bendamustine

Generic: bendamustine hcl
NDC Package

Package Facts

Identity

Package NDC 71288-102-10
Digits Only 7128810210
Product NDC 71288-102
Product ID 71288-102_f9917f10-8be6-4e83-b4d2-cc1fda074337
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-102-10) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-06-05
Brand bendamustine
Generic bendamustine hcl
Sample Package No

Linked Drug Pages (1)

Bendamustine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "f9917f10-8be6-4e83-b4d2-cc1fda074337", "openfda": {"unii": ["981Y8SX18M"], "rxcui": ["1805001", "1805007"], "spl_set_id": ["40f6f58d-d9ac-4f65-9fc7-16984bf1f180"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-102-10)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-102-10", "marketing_start_date": "20230605"}], "brand_name": "Bendamustine", "product_id": "71288-102_f9917f10-8be6-4e83-b4d2-cc1fda074337", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "71288-102", "generic_name": "bendamustine HCl", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bendamustine", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "25 mg/5mL"}], "application_number": "ANDA211001", "marketing_category": "ANDA", "marketing_start_date": "20230605", "listing_expiration_date": "20261231"}