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 20 of 158 · 3,155 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti Bacterial Hand Gel Eucalyptus Rain ALCOHOL Bath & Body Works, Inc. 552ff8dc-b386-0c47-e063-6394a90a47c3 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Waikiki Beach Coconut ALCOHOL Bath & Body Works, Inc. 552fe62e-5e1d-1fed-e063-6294a90a489e 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Pineapple Sunrise ALCOHOL Bath & Body Works, Inc. 552fed13-f326-27bc-e063-6294a90ae131 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Moisturizing Hand Sanitizer Coconut Pina Colada ALCOHOL Bath & Body Works, Inc. 552fe733-25f7-30a7-e063-6294a90a4464 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 552fed13-f323-27bc-e063-6294a90ae131 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Firecracker Pop ALCOHOL Bath & Body Works, Inc. 552ff8dc-b388-0c47-e063-6394a90a47c3 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Japanese Cherry Blossom ALCOHOL Bath & Body Works, Inc. 552fe733-25f9-30a7-e063-6294a90a4464 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pineapple Mango ALCOHOL Bath & Body Works, Inc. 552fe733-25fc-30a7-e063-6294a90a4464 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Peach Blossom and Nectar ALCOHOL Bath & Body Works, Inc. 552feb22-c34c-0572-e063-6394a90afa8c 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Butterfly ALCOHOL Bath & Body Works, Inc. 552ff81f-28d9-0f6e-e063-6394a90ab583 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Strawberry Kiwi ALCOHOL Bath & Body Works, Inc. 552fe584-b74d-00ad-e063-6394a90a68e7 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Cut Lilacs ALCOHOL Bath & Body Works, Inc. 552feb22-c353-0572-e063-6394a90afa8c 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Kiwi Berry ALCOHOL Bath & Body Works, Inc. 552ff8dc-b387-0c47-e063-6394a90a47c3 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Watermelon ALCOHOL Bath & Body Works, Inc. 552fed13-f329-27bc-e063-6294a90ae131 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Neapolitan Ice Cream ALCOHOL Bath & Body Works, Inc. 552ff8dc-b38a-0c47-e063-6394a90a47c3 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Peach Blossom ALCOHOL Bath & Body Works, Inc. 552fe6d9-3364-0842-e063-6394a90a9845 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Iced Lemon Pound Cake Pistachio Milk and Honey ALCOHOL Bath & Body Works, Inc. 552fe73b-38dc-0c49-e063-6394a90a6474 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Cozy Vanilla Almond ALCOHOL Bath & Body Works, Inc. 55300198-e9c1-4539-e063-6294a90a90f1 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pina Colada Swirl ALCOHOL Bath & Body Works, Inc. 552ffde3-ccce-2ffd-e063-6394a90a0840 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Ghoul Friend ALCOHOL Bath & Body Works, Inc. 55300198-e9bc-4539-e063-6294a90a90f1 2026-06-26 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.