🇺🇸
United States · US · US:0078-0684_b8a1cc48-9aaf-486a-9305-090acccb5c02
PROMACTA
Orange BookUNIISPLATC B02BX
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNovartis Pharmaceuticals Corporation
CountryUS (United States)
ATC codeB02BX
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11007806841530 TABLET, FILM COATED in 1 BOTTLE (0078-0684-15)
Annotations
UNII (FDA Substance ID)
4U07F515LG
ELTROMBOPAG OLAMINE
RxCUI 735651
Orange Book
N022291
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4U07F515LG",
"rxcui": "735651",
"inchikey": "PLILLUUXAVKBPY-SBIAVEDLSA-N",
"display_name": "ELTROMBOPAG OLAMINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"7714a0ed-34bb-46e6-a0a5-b363908b22c2": {
"match": "brand_token",
"title": "PROMACTA (ELTROMBOPAG OLAMINE) TABLET, FILM COATED PROMACTA (ELTROMBOPAG OLAMINE) POWDER, FOR SUSPENSION [NOVARTIS PHARMACEUTICALS CORPORATION]",
"spl_version": "31",
"published_date": "2025-12-19"
}
},
"productid": "0078-0684_b8a1cc48-9aaf-486a-9305-090acccb5c02",
"productndc": "0078-0684",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "022291",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "EQ 25MG ACID",
"product_no": "001",
"approval_date": "Nov 20, 2008"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "EQ 50MG ACID",
"product_no": "002",
"approval_date": "Nov 20, 2008"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "EQ 75MG ACID",
"product_no": "003",
"approval_date": "Sep 8, 2009"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "EQ 12.5MG ACID",
"product_no": "004",
"approval_date": "Oct 20, 2011"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "EQ 100MG ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
"product_no": "005",
"approval_date": "Nov 16, 2012"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ELTROMBOPAG OLAMINE",
"proprietary_name": "PROMACTA",
"active_ingred_unit": "mg/1",
"application_number": "NDA022291",
"marketing_category": "NDA",
"nonproprietary_name": "eltrombopag olamine",
"start_marketing_date": "20160822",
"active_numerator_strength": "12.5"
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