Package 69945-120-56

Brand: thallous chloride tl 201

Generic: thallous chloride, tl 201
NDC Package

Package Facts

Identity

Package NDC 69945-120-56
Digits Only 6994512056
Product NDC 69945-120
Description

1 VIAL in 1 CAN (69945-120-56) / 5.6 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2015-11-04
Brand thallous chloride tl 201
Generic thallous chloride, tl 201
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "468f144a-9b53-8989-e063-6294a90a9541", "openfda": {"unii": ["3I8Y076A0E"], "spl_set_id": ["0da81fc0-a137-46d3-9378-d8053a82e61a"], "manufacturer_name": ["Curium US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CAN (69945-120-56)  / 5.6 mL in 1 VIAL", "package_ndc": "69945-120-56", "marketing_start_date": "20151104"}], "brand_name": "THALLOUS CHLORIDE Tl 201", "product_id": "69945-120_468f144a-9b53-8989-e063-6294a90a9541", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Radioactive Diagnostic Agent [EPC]", "Radiopharmaceutical Activity [MoA]"], "product_ndc": "69945-120", "generic_name": "thallous chloride, Tl 201", "labeler_name": "Curium US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "THALLOUS CHLORIDE Tl 201", "active_ingredients": [{"name": "THALLOUS CHLORIDE TL-201", "strength": "1 mCi/mL"}], "application_number": "NDA018150", "marketing_category": "NDA", "marketing_start_date": "20151104", "listing_expiration_date": "20261231"}