Package 0270-7097-08

Brand: lumason

Generic: sulfur hexafluoride
NDC Package

Package Facts

Identity

Package NDC 0270-7097-08
Digits Only 0270709708
Product NDC 0270-7097
Description

20 VIAL in 1 BOX (0270-7097-08) / 25 mg in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-04-01
Brand lumason
Generic sulfur hexafluoride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "INTRAVESICAL"], "spl_id": "47b0f2df-0b6c-a221-750d-763d5ece665b", "openfda": {"nui": ["N0000175864", "N0000010259"], "unii": ["EAG959U971", "841B886EJ7", "WS7LR3I1D6"], "spl_set_id": ["69822a55-226c-f133-e3b8-2b5826667c5b"], "pharm_class_epc": ["Contrast Agent for Ultrasound Imaging [EPC]"], "pharm_class_moa": ["Ultrasound Contrast Activity [MoA]"], "manufacturer_name": ["BRACCO DIAGNOSTICS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL in 1 BOX (0270-7097-08)  / 25 mg in 1 VIAL", "package_ndc": "0270-7097-08", "marketing_start_date": "20210401"}], "brand_name": "Lumason", "product_id": "0270-7097_47b0f2df-0b6c-a221-750d-763d5ece665b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION", "pharm_class": ["Contrast Agent for Ultrasound Imaging [EPC]", "Ultrasound Contrast Activity [MoA]"], "product_ndc": "0270-7097", "generic_name": "SULFUR HEXAFLUORIDE", "labeler_name": "BRACCO DIAGNOSTICS INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lumason", "active_ingredients": [{"name": "DISTEAROYLPHOSPHATIDYLCHOLINE, DL-", "strength": ".19 mg/mg"}, {"name": "SODIUM 1,2-DIPALMITOYL-SN-GLYCERO-3-PHOSPHO-(1'-RAC-GLYCEROL)", "strength": ".19 mg/mg"}, {"name": "SULFUR HEXAFLUORIDE", "strength": "60.7 mg/mg"}], "application_number": "NDA203684", "marketing_category": "NDA", "marketing_start_date": "20210401", "listing_expiration_date": "20261231"}