Package 59353-002-10

Brand: retacrit

Generic: epoetin alfa-epbx
NDC Package

Package Facts

Identity

Package NDC 59353-002-10
Digits Only 5935300210
Product NDC 59353-002
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (59353-002-10) / 1 mL in 1 VIAL, SINGLE-DOSE (59353-002-01)

Marketing

Marketing Status
Marketed Since 2018-06-18
Brand retacrit
Generic epoetin alfa-epbx
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "5626304b-344f-4155-9afa-d7cfe733d819", "openfda": {"unii": ["64FS3BFH5W"], "rxcui": ["2047591", "2047596", "2047600", "2047602", "2047606", "2047608", "2047612", "2047614", "2463731", "2463733", "2463735", "2463737"], "spl_set_id": ["e6e4dd0c-25ca-40b2-ba6b-6138a68621fe"], "manufacturer_name": ["Vifor (International) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (59353-002-10)  / 1 mL in 1 VIAL, SINGLE-DOSE (59353-002-01)", "package_ndc": "59353-002-10", "marketing_start_date": "20180618"}], "brand_name": "RETACRIT", "product_id": "59353-002_5626304b-344f-4155-9afa-d7cfe733d819", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Erythropoiesis-stimulating Agent [EPC]", "Erythropoietin [CS]", "Increased Erythroid Cell Production [PE]"], "product_ndc": "59353-002", "generic_name": "epoetin alfa-epbx", "labeler_name": "Vifor (International) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RETACRIT", "active_ingredients": [{"name": "EPOETIN", "strength": "2000 [iU]/mL"}], "application_number": "BLA125545", "marketing_category": "BLA", "marketing_start_date": "20180618", "listing_expiration_date": "20261231"}