Package 0003-2187-13

Brand: orencia

Generic: abatacept
NDC Package

Package Facts

Identity

Package NDC 0003-2187-13
Digits Only 0003218713
Product NDC 0003-2187
Description

1 VIAL, SINGLE-USE in 1 CARTON (0003-2187-13) / 15 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2009-01-01
Brand orencia
Generic abatacept
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "962695b7-21f5-44bb-80e0-cb3b48c80be6", "openfda": {"nui": ["N0000008571", "N0000182159", "M0018640"], "unii": ["7D0YB67S97"], "rxcui": ["616015", "616018", "1145929", "1145932", "1799228", "1799230", "1925254", "1925255", "1925256", "1925257"], "spl_set_id": ["0836c6ac-ee37-5640-2fed-a3185a0b16eb"], "pharm_class_cs": ["Recombinant Fusion Proteins [CS]"], "pharm_class_pe": ["Decreased Cytokine Activity [PE]"], "pharm_class_epc": ["Selective T Cell Costimulation Modulator [EPC]"], "manufacturer_name": ["E.R. Squibb & Sons, L.L.C."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0003-2187-13)  / 15 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0003-2187-13", "marketing_start_date": "20090101"}], "brand_name": "ORENCIA", "product_id": "0003-2187_962695b7-21f5-44bb-80e0-cb3b48c80be6", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Decreased Cytokine Activity [PE]", "Recombinant Fusion Proteins [CS]", "Selective T Cell Costimulation Modulator [EPC]"], "product_ndc": "0003-2187", "generic_name": "abatacept", "labeler_name": "E.R. Squibb & Sons, L.L.C.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ORENCIA", "active_ingredients": [{"name": "ABATACEPT", "strength": "250 mg/15mL"}], "application_number": "BLA125118", "marketing_category": "BLA", "marketing_start_date": "20090101", "listing_expiration_date": "20261231"}