FDA.reportPublic FDA data

NDC 0074-0010-01 - Lupron Depot-PED

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0074-0010
Requested NDC
0074-0010-01
Package NDCs from labels
0074-0010-01
Manufacturer
AbbVie Inc.
Effective date
2025-11-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lupron Depot-PED - AbbVie Inc.AbbVie Inc.2025-11-14HUMAN PRESCRIPTION DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0074-0010LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]93Unmatched20241109_e99f47d2-da10-3127-ecb3-e5d942ae6e81.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LEUPROLIDE ACETATEACTIVE INGREDIENT37JNS02E7VLUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
LEUPROLIDEACTIVE MOIETYEFY6W0M8TGLUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
ACETIC ACIDINACTIVE INGREDIENTQ40Q9N063PLUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS311LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
MANNITOLINACTIVE INGREDIENT3OWL53L36ALUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
POLYLACTIDEINACTIVE INGREDIENT459TN2L5F5LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HLUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36
WATERINACTIVE INGREDIENT059QF0KO0RLUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.]36

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 26 of 49 · 968 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Xpect Alcohol WipesALCOHOL WIPESCintas Corporation51185b9a-ed6b-4a49-b524-b3ff0d5c62902025-09-29WarningsExact identifier
unii: ND2M416302
CheBoho TEA TREE ACNECHEBOHO TEA TREE ACNEOpalshi(Guangzhou)E-commerce Co. Ltd.3fc4cf84-b2da-c593-e063-6394a90abc5c2025-09-27WarningsExact identifier
unii: 059QF0KO0R
FensolviLEUPROLIDE ACETATETOLMAR Inc.2c311700-edf4-4f2a-a468-9875489a6cc72025-09-25Warnings, Adverse reactionsExact identifier
unii: 37JNS02E7V
HUMCO 1 Percent IodineISOPROPYL ALCOHOLHumco Holding Group, Inc.139efeef-be20-4362-a5ba-158b8fa40e0d2025-09-22WarningsExact identifier
unii: ND2M416302
Xpect Isopropyl AlcoholISOPROPYL ALCOHOLCintas Corpb55fe473-45d2-48d3-b4d4-fc0993cb4dfe2025-09-22WarningsExact identifier
unii: ND2M416302
Sterile WaterWATERProPharma Distribution3f2ae880-852f-b45d-e063-6394a90aa1cc2025-09-19Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
REFRESH OPTIVE DropsCARBOXYMETHYLCELLULOSE SODIUM AND GLYCERINAllergan, Inc.80275190-d717-40ea-905b-5c8fbe986eac2025-09-15WarningsExact identifier
unii: K679OBS311
Refresh Relieva PF XtraCARBOXYMETHYLCELLULOSE SODIUM AND GLYCERINAllergan, Inc.b51b8a75-8faa-430f-8f7e-ee58d3d13f2e2025-09-15WarningsExact identifier
unii: K679OBS311
Refresh RelievaCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINAllergan, Inc.6b984fa2-4187-45ef-b7d3-15e720abc6672025-09-15WarningsExact identifier
unii: K679OBS311
Lubricant DropsCARBOXYMETHYLCELLULOSE SODIUMCARDINAL HEALTH 110, LLC. DBA LEADER1ac2fe24-9ff6-48c1-b123-fbc0e48f53042025-09-12WarningsExact identifier
unii: K679OBS311
Dry Eye ReliefCARBOXYMETHYLCELLULOSE SODIUMCARDINAL HEALTH 110, LLC. DBA LEADERbd262028-32e9-052d-e053-2a95a90a53032025-09-12WarningsExact identifier
unii: K679OBS311
Medi-First First Aid Eye WashPURIFIED WATERUnifirst First Aid Corporationdcd7fe56-ff5c-4c8d-a415-6e363d7e53f42025-09-08WarningsExact identifier
unii: 059QF0KO0R
Green Guard First Aid Eye WashWATERUnifirst First Aid Corporationa4ba5526-b4e2-4bcc-9127-aa22ebf5017f2025-09-08WarningsExact identifier
unii: 059QF0KO0R
Medi-First Plus First Aid Eye WashWATERUnifirst First Aid Corporationd7ea80ca-b4a0-4476-8b50-b3425c6d456a2025-09-08WarningsExact identifier
unii: 059QF0KO0R
ECOLAB Eye WashPURIFIED WATERECOLAB Food Safety Specialties, Inc.4bcfa21a-791e-4d04-e054-00144ff88e882025-09-08WarningsExact identifier
unii: 059QF0KO0R
Medi-First Plus Alcohol Wipes70% ISOPROPYL ALCOHOLUnifirst First Aid Corporation3f507990-282a-4b26-e054-00144ff8d46c2025-09-08WarningsExact identifier
unii: ND2M416302
Green Guard Sterile Alcohol WipesISOPROPYL ALCOHOL 70%Unifirst First Aid Corporation570baa70-e519-328b-e054-00144ff8d46c2025-09-08WarningsExact identifier
unii: ND2M416302
Medi-First Alcohol WipesISOPROPYL ALCOHOLUnifirst First Aid Corporationce650cb6-5398-29e7-e053-2995a90ac7972025-09-08WarningsExact identifier
unii: ND2M416302
Medi-First Sting ReliefBENZOCAINE 6%, ISOPROPYL ALCOHOL 60%Unifirst First Aid Corporation6e610821-b030-930b-e053-2a91aa0a66f92025-09-08WarningsExact identifier
unii: ND2M416302
Medi-First Isopropyl AlcoholISOPROPYL ALCOHOLUnifirst First Aid Corporationdbee035e-094f-f8a3-e053-2995a90a66202025-09-08WarningsExact identifier
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.