Package 72893-007-04

Brand: zevalin

Generic: ibritumomab tiuxetan
NDC Package

Package Facts

Identity

Package NDC 72893-007-04
Digits Only 7289300704
Product NDC 72893-007
Description

1 KIT in 1 CARTON (72893-007-04) * 10 mL in 1 VIAL * 2 mL in 1 VIAL * 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2002-02-19
Brand zevalin
Generic ibritumomab tiuxetan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "c1ec6e37-45bb-4cda-a821-464552c48982", "openfda": {"spl_set_id": ["25d367dc-da65-44c9-a844-1bf15339c285"], "manufacturer_name": ["Acrotech Biopharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72893-007-04)  *  10 mL in 1 VIAL *  2 mL in 1 VIAL *  2 mL in 1 VIAL", "package_ndc": "72893-007-04", "marketing_start_date": "20020219"}], "brand_name": "Zevalin", "product_id": "72893-007_c1ec6e37-45bb-4cda-a821-464552c48982", "dosage_form": "KIT", "product_ndc": "72893-007", "generic_name": "ibritumomab tiuxetan", "labeler_name": "Acrotech Biopharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zevalin", "application_number": "BLA125019", "marketing_category": "BLA", "marketing_start_date": "20020219", "listing_expiration_date": "20261231"}