NDC 0078-0804 - Sandostatin LAR Depot

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
0078-0804
Package NDCs from labels
0078-0804-61
Manufacturer
Novartis Pharmaceuticals Corporation
Effective date
2025-12-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sandostatin LAR Depot - Novartis Pharmaceuticals CorporationNovartis Pharmaceuticals Corporation2025-12-22HUMAN PRESCRIPTION DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0078-0804SANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]25Unmatched20240723_d0b7fe9e-7000-4b79-ba3b-291ce92c14f9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M416302SANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
OCTREOTIDE ACETATEACTIVE INGREDIENT75R0U2568ISANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
ISOPROPYL ALCOHOLACTIVE MOIETYND2M416302SANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
OCTREOTIDEACTIVE MOIETYRWM8CCW8GPSANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS311SANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
LACTIC ACID, DL-INACTIVE INGREDIENT3B8D35Y7S4SANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
MANNITOLINACTIVE INGREDIENT3OWL53L36ASANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
POLOXAMER 188INACTIVE INGREDIENTLQA7B6G8JGSANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12
WATERINACTIVE INGREDIENT059QF0KO0RSANDOSTATIN LAR DEPOT (OCTREOTIDE ACETATE) KIT SANDOSTATIN LAR DEPOT DEMONSTRATION KIT (OCTREOTIDE ACETATE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]12

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 17 of 17 · 326 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dynamic Eyewash with EyecupWATERDynamic Safety International7d3af0f4-0e1f-9ea5-e053-2991aa0af7a22018-12-17WarningsExact identifier
unii: 059QF0KO0R
Bio Rock WaterROCK WATERBioActive Nutritional, Inc.178bd16d-0d4f-49d8-866b-8ab3a3c6889d2018-07-30WarningsExact identifier
unii: 059QF0KO0R
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: 3B8D35Y7S4
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.