Package 0270-7099-73

Brand: lumason

Generic: sulfur hexafluoride
NDC Package

Package Facts

Identity

Package NDC 0270-7099-73
Digits Only 0270709973
Product NDC 0270-7099
Product ID 0270-7099_47b0f2df-0b6c-a221-750d-763d5ece665b
Description

5 KIT in 1 BOX (0270-7099-73) / 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2020-01-15
Brand lumason
Generic sulfur hexafluoride
Sample Package No

Linked Drug Pages (1)

Lumason, LumaSon ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"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": "5 KIT in 1 BOX (0270-7099-73)  / 1 KIT in 1 KIT *  25 mg in 1 VIAL *  5 mL in 1 SYRINGE", "package_ndc": "0270-7099-73", "marketing_start_date": "20200115"}], "brand_name": "LumaSon", "product_id": "0270-7099_47b0f2df-0b6c-a221-750d-763d5ece665b", "dosage_form": "KIT", "product_ndc": "0270-7099", "generic_name": "SULFUR HEXAFLUORIDE", "labeler_name": "BRACCO DIAGNOSTICS INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LumaSon", "application_number": "NDA203684", "marketing_category": "NDA", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}