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United States · US · US:0078-0249_f052c25a-d848-4b2d-8ff3-73bee0c89ad7
Femara
Orange BookUNIISPLATC L02BG04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNovartis Pharmaceuticals Corporation
CountryUS (United States)
ATC codeL02BG04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11007802491530 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0249-15)
Annotations
UNII (FDA Substance ID)
7LKK855W8I
LETROZOLE
RxCUI 72965
Orange Book
N020726
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7LKK855W8I",
"rxcui": "72965",
"inchikey": "HPJKCIUCZWXJDR-UHFFFAOYSA-N",
"display_name": "LETROZOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"82b77d74-085f-45ac-a7dd-1f5c038bf406": {
"match": "brand_token",
"title": "FEMARA (LETROZOLE) TABLET, FILM COATED [NOVARTIS PHARMACEUTICALS CORPORATION]",
"spl_version": "31",
"published_date": "2025-08-25"
}
},
"productid": "0078-0249_f052c25a-d848-4b2d-8ff3-73bee0c89ad7",
"productndc": "0078-0249",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "020726",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "Jul 25, 1997"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LETROZOLE",
"proprietary_name": "Femara",
"active_ingred_unit": "mg/1",
"application_number": "NDA020726",
"marketing_category": "NDA",
"nonproprietary_name": "letrozole",
"start_marketing_date": "19970731",
"active_numerator_strength": "2.5"
}Related drugs
Other records sharing ATC code L02BG04.
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