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United States · US · US:0074-3641_691f9b76-b15b-47c9-8df9-8ebe91999b45
Lupron Depot
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAbbVie Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1100743641031 KIT in 1 CARTON (0074-3641-03) * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET
- ndc1100743641711 KIT in 1 CARTON (0074-3641-71) * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET
Annotations
Orange Book
N020011
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"e99f47d2-da10-3127-ecb3-e5d942ae6e81": {
"match": "brand_token",
"title": "LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]",
"spl_version": "97",
"published_date": "2025-11-26"
}
},
"productid": "0074-3641_691f9b76-b15b-47c9-8df9-8ebe91999b45",
"productndc": "0074-3641",
"dosage_form": "KIT",
"orange_book": {
"appl_no": "020011",
"products": [
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "3.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
"product_no": "001",
"approval_date": "Oct 22, 1990"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "3.75MG",
"product_no": "002",
"approval_date": "Oct 26, 1995"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "Lupron Depot",
"active_ingred_unit": null,
"application_number": "NDA020011",
"marketing_category": "NDA",
"nonproprietary_name": "leuprolide acetate",
"start_marketing_date": "19901022",
"active_numerator_strength": null
}Access this data programmatically
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