🇺🇸
United States · US · US:73302-456_47d0b808-7143-c7a9-e063-6394a90a6e0d
Ella
Orange BookUNIISPLATC G03XB02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHRA PHARMA AMERICA, INC.
CountryUS (United States)
ATC codeG03XB02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1173302456011 BLISTER PACK in 1 CARTON (73302-456-01) / 1 TABLET in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
YF7V70N02B
ULIPRISTAL ACETATE
RxCUI 1005920
Orange Book
N022474
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "YF7V70N02B",
"rxcui": "1005920",
"inchikey": "OOLLAFOLCSJHRE-ZHAKMVSLSA-N",
"display_name": "ULIPRISTAL ACETATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"2bf93d23-cddd-4613-9066-5b5fa090404b": {
"match": "brand_token",
"title": "ELLA (ULIPRISTAL ACETATE) TABLET [HRA PHARMA AMERICA, INC.]",
"spl_version": "6",
"published_date": "2026-01-08"
}
},
"productid": "73302-456_47d0b808-7143-c7a9-e063-6394a90a6e0d",
"productndc": "73302-456",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "022474",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "30MG",
"product_no": "001",
"approval_date": "Aug 13, 2010"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ULIPRISTAL ACETATE",
"proprietary_name": "Ella",
"active_ingred_unit": "mg/1",
"application_number": "NDA022474",
"marketing_category": "NDA",
"nonproprietary_name": "ulipristal acetate",
"start_marketing_date": "20200511",
"active_numerator_strength": "30"
}Related drugs
Other records sharing ATC code G03XB02.
Access this data programmatically
Query Ella and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.