FDA.reportPublic FDA data

NDC 0074-0010 - 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
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 49 of 49 · 968 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bio Rock WaterROCK WATERBioActive Nutritional, Inc.178bd16d-0d4f-49d8-866b-8ab3a3c6889d2018-07-30WarningsExact identifier
unii: 059QF0KO0R
Acetic AcidACETIC ACIDBaxter Healthcare Corporation41bc12af-fac5-4ac1-b907-dcb3e35a054c2018-02-02Warnings, Adverse reactionsExact identifier
unii: Q40Q9N063P
ENT Essentials All Dry Ear Drying DropsISOPROPYL ALCOHOLWisconsin Pharmacal Company5f0bb412-577e-3155-e053-2a91aa0a7f532017-11-28WarningsExact identifier
unii: ND2M416302
Homeoplex DGLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,Supplement Clinic, LLC.cd6b48ab-3566-484d-8deb-15ef6f8e7e8f2017-11-01WarningsExact identifier
unii: Q40Q9N063P
Glucose Control T015SYZYGIUM JAMBOLANUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, HYPOPHYSIS SUIS, PANCREAS SUIS, PHASEOLUS, ACETICUM ACIDUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, URANIUM NITRICUMGuangzhou Renuma Medical Systems Co., Ltd3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b2017-10-26WarningsExact identifier
unii: Q40Q9N063P
Sterile WaterWATERBaxter Healthcare Corporationef3e79c5-3f58-4b36-a296-64b7d9a651c12017-10-17Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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