Package 50242-053-06

Brand: rituxan

Generic: rituximab
NDC Package

Package Facts

Identity

Package NDC 50242-053-06
Digits Only 5024205306
Product NDC 50242-053
Product ID 50242-053_3a716937-c2af-4bf9-976c-c34746b22ff0
Description

1 VIAL, SINGLE-USE in 1 CARTON (50242-053-06) / 50 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 1997-11-26
Brand rituxan
Generic rituximab
Sample Package No

Linked Drug Pages (1)

Rituxan ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "3a716937-c2af-4bf9-976c-c34746b22ff0", "openfda": {"nui": ["N0000175078", "N0000175657"], "unii": ["4F4X42SYQ6"], "rxcui": ["1657862", "1657864", "1657867", "1657868"], "spl_set_id": ["b172773b-3905-4a1c-ad95-bab4b6126563"], "pharm_class_epc": ["CD20-directed Cytolytic Antibody [EPC]"], "pharm_class_moa": ["CD20-directed Antibody Interactions [MoA]"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (50242-053-06)  / 50 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50242-053-06", "marketing_start_date": "19971126"}], "brand_name": "Rituxan", "product_id": "50242-053_3a716937-c2af-4bf9-976c-c34746b22ff0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["CD20-directed Antibody Interactions [MoA]", "CD20-directed Cytolytic Antibody [EPC]"], "product_ndc": "50242-053", "generic_name": "rituximab", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rituxan", "active_ingredients": [{"name": "RITUXIMAB", "strength": "10 mg/mL"}], "application_number": "BLA103705", "marketing_category": "BLA", "marketing_start_date": "19971126", "listing_expiration_date": "20261231"}