Package 80725-610-25

Brand: leukeran

Generic: chlorambucil
NDC Package

Package Facts

Identity

Package NDC 80725-610-25
Digits Only 8072561025
Product NDC 80725-610
Product ID 80725-610_5a3f7aed-1747-4c52-9e10-5aa090dd088e
Description

25 TABLET, FILM COATED in 1 BOTTLE (80725-610-25)

Marketing

Marketing Status
Marketed Since 2023-05-15
Brand leukeran
Generic chlorambucil
Sample Package No

Linked Drug Pages (1)

LEUKERAN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5a3f7aed-1747-4c52-9e10-5aa090dd088e", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["18D0SL7309"], "rxcui": ["105553", "197462"], "spl_set_id": ["58a3c995-5ad6-465d-8437-5970c9088213"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Waylis Therapeutics LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET, FILM COATED in 1 BOTTLE (80725-610-25)", "package_ndc": "80725-610-25", "marketing_start_date": "20230515"}], "brand_name": "LEUKERAN", "product_id": "80725-610_5a3f7aed-1747-4c52-9e10-5aa090dd088e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "80725-610", "generic_name": "chlorambucil", "labeler_name": "Waylis Therapeutics LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEUKERAN", "active_ingredients": [{"name": "CHLORAMBUCIL", "strength": "2 mg/1"}], "application_number": "NDA010669", "marketing_category": "NDA", "marketing_start_date": "20230515", "listing_expiration_date": "20261231"}