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United States · US · US:17156-021_bc294a45-4008-4476-b7a4-9475b18d43a2
Indium in 111 Oxyquinoline
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMedi-Physics Inc. dba GE Healthcare.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1117156021011 VIAL in 1 BOX (17156-021-01) / 1 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
LGX9OL562T
INDIUM IN-111 OXYQUINOLINE
RxCUI 1314372
Orange Book
N019044
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "LGX9OL562T",
"rxcui": "1314372",
"inchikey": "AEGSYIKLTCZUEZ-UHFFFAOYSA-K",
"display_name": "INDIUM IN-111 OXYQUINOLINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"7dbfc0f9-0e2e-4aed-85bd-32cf7c74d402": {
"match": "brand_token",
"title": "INDIUM IN 111 OXYQUINOLINE (INDIUM IN-111 OXYQUINOLINE) LIQUID [BWXT MEDICAL LTD.]",
"spl_version": "4",
"published_date": "2024-11-06"
}
},
"productid": "17156-021_bc294a45-4008-4476-b7a4-9475b18d43a2",
"productndc": "17156-021",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "019044",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AP",
"strength": "1mCi/ML",
"product_no": "001",
"approval_date": "Dec 24, 1985"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "INDIUM IN-111 OXYQUINOLINE",
"proprietary_name": "Indium in 111 Oxyquinoline",
"active_ingred_unit": "ug/mL",
"application_number": "NDA019044",
"marketing_category": "NDA",
"nonproprietary_name": "Indium In-111 Oxyquinoline",
"start_marketing_date": "19851201",
"active_numerator_strength": "1"
}Access this data programmatically
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