Package 72536-0920-1

Brand: indium in 111 oxyquinoline

Generic: indium in-111 oxyquinoline
NDC Package

Package Facts

Identity

Package NDC 72536-0920-1
Digits Only 7253609201
Product NDC 72536-0920
Description

1 mL in 1 VIAL, SINGLE-DOSE (72536-0920-1)

Marketing

Marketing Status
Marketed Since 2019-09-27
Brand indium in 111 oxyquinoline
Generic indium in-111 oxyquinoline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0864f662-e3ce-4426-8c3c-e318f755a89d", "openfda": {"nui": ["N0000177914", "N0000000205"], "unii": ["LGX9OL562T"], "spl_set_id": ["7dbfc0f9-0e2e-4aed-85bd-32cf7c74d402"], "pharm_class_epc": ["Radioactive Diagnostic Agent [EPC]"], "pharm_class_moa": ["Radiopharmaceutical Activity [MoA]"], "manufacturer_name": ["BWXT Medical Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (72536-0920-1)", "package_ndc": "72536-0920-1", "marketing_start_date": "20190927"}], "brand_name": "Indium In 111 Oxyquinoline", "product_id": "72536-0920_0864f662-e3ce-4426-8c3c-e318f755a89d", "dosage_form": "LIQUID", "product_ndc": "72536-0920", "generic_name": "Indium In-111 Oxyquinoline", "labeler_name": "BWXT Medical Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Indium In 111 Oxyquinoline", "active_ingredients": [{"name": "INDIUM IN-111 OXYQUINOLINE", "strength": "1 mCi/mL"}], "application_number": "ANDA202586", "marketing_category": "ANDA", "marketing_start_date": "20190927", "listing_expiration_date": "20261231"}