Package 0270-7099-16
Brand: lumason
Generic: sulfur hexafluoridePackage Facts
Identity
Package NDC
0270-7099-16
Digits Only
0270709916
Product NDC
0270-7099
Description
5 KIT in 1 BOX (0270-7099-16) / 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGE
Marketing
Marketing Status
Brand
lumason
Generic
sulfur hexafluoride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "5407234f-5a9d-9a66-2e42-6629c0c74aec", "openfda": {"nui": ["N0000175864", "N0000010259"], "unii": ["EAG959U971", "841B886EJ7", "WS7LR3I1D6"], "spl_set_id": ["7c679424-c3f7-ed02-892f-20ca0d775089"], "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 (0270-7099-16) / 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGE", "package_ndc": "0270-7099-16", "marketing_start_date": "20150115"}], "brand_name": "LumaSon", "product_id": "0270-7099_5407234f-5a9d-9a66-2e42-6629c0c74aec", "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": "20150115", "listing_expiration_date": "20261231"}