Package 50242-105-01

Brand: polivy

Generic: polatuzumab vedotin
NDC Package

Package Facts

Identity

Package NDC 50242-105-01
Digits Only 5024210501
Product NDC 50242-105
Product ID 50242-105_f7a11f1f-8a77-4220-9337-14c4dbc6e0dc
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (50242-105-01) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2019-06-10
Brand polivy
Generic polatuzumab vedotin
Sample Package No

Linked Drug Pages (1)

POLIVY ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "f7a11f1f-8a77-4220-9337-14c4dbc6e0dc", "openfda": {"unii": ["KG6VO684Z6"], "rxcui": ["2174095", "2174100", "2398131", "2398133"], "spl_set_id": ["20a16ab2-f338-4abb-9dcd-254bd949a2bc"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (50242-105-01)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50242-105-01", "marketing_start_date": "20190610"}], "brand_name": "POLIVY", "product_id": "50242-105_f7a11f1f-8a77-4220-9337-14c4dbc6e0dc", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "product_ndc": "50242-105", "generic_name": "polatuzumab vedotin", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POLIVY", "active_ingredients": [{"name": "POLATUZUMAB VEDOTIN", "strength": "140 mg/7.52mL"}], "application_number": "BLA761121", "marketing_category": "BLA", "marketing_start_date": "20190610", "listing_expiration_date": "20261231"}