Home NDC 68875-0102-01 NDC 68875-0102-01 - Gattex 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 68875-0102
Requested NDC 68875-0102-01
Package NDCs from labels 68875-0102-1, 68875-0102-01
Manufacturer Takeda Pharmaceuticals America, Inc.
Effective date 2025-09-05
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68875-0101-1 Gattex 0.5 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 15 mL 5 mg in 0.5mL 20 68875-0102-1 Gattex 1 in 1 CARTON KIT 1 20
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68875-0102 GATTEX (TEDUGLUTIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [TAKEDA PHARMACEUTICALS AMERICA, INC.] 19 Current NDC, Legacy NDC, 2 package rows 20241003_66b69c1e-b25c-44d3-b5ff-1c1de9a516fa.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded teduglutide ACTIVE INGREDIENT 7M19191IKG GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3 water ACTIVE INGREDIENT 059QF0KO0R GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3 teduglutide ACTIVE MOIETY 7M19191IKG GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3 water ACTIVE MOIETY 059QF0KO0R GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3 Histidine INACTIVE INGREDIENT 4QD397987E GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3 mannitol INACTIVE INGREDIENT 3OWL53L36A GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3 sodium phosphate, dibasic, heptahydrate INACTIVE INGREDIENT 70WT22SF4B GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3 sodium phosphate, monobasic, monohydrate INACTIVE INGREDIENT 593YOG76RN GATTEX (TEDUGLUTIDE) INJECTION, POWDER, FOR SOLUTION GATTEX (TEDUGLUTIDE) KIT [NPS PHARMACEUTICALS] 3
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 124 of 156 · 3,113 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hand LOTION Derma Glove 93736944-7535-4035-93aa-4771138af8e3 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Relief LOTION Derma Glove 39867f66-b641-4060-881d-161c2591d19c 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Relief LOTION Derma Glove 767cc1f2-89a2-4d0b-ae49-ad7b9afca18b 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Recovery ALCOHOL Derma Glove b4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand LOTION Derma Glove 1c46e4da-7594-48b0-8e8d-803189118420 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Sanitizer HAND SANITIZER UNSCENTED CASAD Company, Inc 07a891a3-dcf7-438f-bbf7-a20b2aa7d7d7 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Mist ALCOHOL Derma Glove dd849fb3-95af-4a32-9687-3b966d456fbb 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Sanitizer HAND SANITIZER UNSCENTED CASAD Company, Inc 0933de73-94b1-448e-b39f-ecffabf95288 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Recovery ALCOHOL Derma Glove d8705086-7209-4f13-bd54-604c90495f0a 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand LOTION Derma Glove d158394e-baec-4770-8ee8-19285722ca61 2024-10-09 Warnings Exact identifier unii: 3K9958V90M FOAMING HAND ALCOHOL FOAM ALCOHOL Draco Hygienic Products Inc. 14860a19-e1e8-71fc-e063-6394a90a9df8 2024-10-08 Warnings Exact identifier unii: 3K9958V90M Germ Attack Hand Sanitizer ALCOHOL Natural Essentials, Inc. 4d156264-566d-4516-876c-b6f5823a97f5 2024-10-04 Warnings Exact identifier unii: 3K9958V90M Germ Attack Hand Sanitizer ALCOHOL Natural Essentials, Inc. 9d3a4dfe-f31d-4def-bfc2-ece69d13f8e4 2024-10-04 Warnings Exact identifier unii: 3K9958V90M Saluja MD Essential Hand Sanitizer ETHYL ALCOHOL Anita Saluja, Md, LLC 5c112afc-2a3d-46b2-94a8-830e8ff83044 2024-10-04 Warnings Exact identifier unii: 3K9958V90M TERUFLEX BLOOD with Diversion Blood Sampling Arm 70 mL CPDA-1 ANHYDROUS CITRIC ACID, TRISODIUM CITRATE DIHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, DEXTROSE MONOHYDRATE, AND ADENINE Terumo Corporation 39f2e11c-5a31-469f-b725-d096c1674421 2024-10-03 Warnings Exact identifier unii: 593YOG76RN Purell ALCOHOL Navajo Manufacturing Company Inc. 969b2968-8497-4125-949a-6be39b132edb 2024-10-02 Warnings Exact identifier unii: 3K9958V90M MY MEDIC SUPER SANITIZER ALCOHOL Nantong Health & Beyond Hygienic Products Inc. f19971b1-2aeb-4c37-82b0-9525026cff7a 2024-10-02 Warnings Exact identifier unii: 3K9958V90M GenRx Anti-Bacterial Gel ALCOHOL PureTek Corporation a124e37e-1a44-212a-e053-2995a90a0af0 2024-10-01 Warnings Exact identifier unii: 3K9958V90M Hand Sanitizing with Lavender Oil ALCOHOL PureTek Corporation a75d25a7-1e23-717f-e053-2a95a90a6d93 2024-10-01 Warnings Exact identifier unii: 3K9958V90M AOSI HEALTHCARE HAND SANITIZER ALCOHOL Nantong Health & Beyond Hygienic Products Inc. 59d631d0-d8ae-45a8-a7a9-26de9cc427b3 2024-09-25 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.