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 18 of 158 · 3,155 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti-BacterialHandSpray Blush Petals ALCOHOL Bath & Body Works, Inc. 552fa251-6e0e-ce9f-e063-6394a90a14e1 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Waikiki Beach Coconut ALCOHOL Bath & Body Works, Inc. 552f9bc7-3158-a502-e063-6294a90a2d71 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Malibu Mist ALCOHOL Bath & Body Works, Inc. 552f9e7b-b278-ce3a-e063-6394a90ae9ab 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Japanese Cherry Blossom ALCOHOL Bath & Body Works, Inc. 552fa3e5-00b8-3825-e063-6294a90a1b0b 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Guava Glow ALCOHOL Bath & Body Works, Inc. 552f9e7b-b275-ce3a-e063-6394a90ae9ab 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Strawberry Bite ALCOHOL Bath & Body Works, Inc. 552f9cd1-3597-e2aa-e063-6294a90a8219 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray In The Stars ALCOHOL Bath & Body Works, Inc. 552fa1b9-497c-cde8-e063-6394a90a89b5 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Japanese Cherry Blossom ALCOHOL Bath & Body Works, Inc. 552f95c9-e6e0-a1d7-e063-6294a90a83d6 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Fresh Watermelon ALCOHOL Bath & Body Works, Inc. 552f9bc7-3159-a502-e063-6294a90a2d71 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Vanilla Whip ALCOHOL Bath & Body Works, Inc. 552fa700-4214-d614-e063-6394a90aa12f 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Disney Princess Belle ALCOHOL Bath & Body Works, Inc. 552fbc4a-1f6c-d72a-e063-6294a90aebb2 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel The Mandalorian and Grogu Bounty Hunter ALCOHOL Bath & Body Works, Inc. 552fbc4a-1f6b-d72a-e063-6294a90aebb2 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Berry Burst ALCOHOL Bath & Body Works, Inc. 552fc4da-f249-e88a-e063-6394a90ae2ab 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fiji White Sands ALCOHOL Bath & Body Works, Inc. 552fbaea-cc8e-ff08-e063-6294a90aa086 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Blue Washed Sky ALCOHOL Bath & Body Works, Inc. 552fc18b-aa5e-e667-e063-6394a90a908e 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Peepin It Real Disney Villains Maleficent ALCOHOL Bath & Body Works, Inc. 552fc18b-aa62-e667-e063-6394a90a908e 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Disney Princess Mulan ALCOHOL Bath & Body Works, Inc. 552fccdd-93bf-efff-e063-6294a90a54ba 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Lifes A Fairytale ALCOHOL Bath & Body Works, Inc. 552fc8da-e387-0dc5-e063-6294a90a9c0c 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sunshine and Lemons ALCOHOL Bath & Body Works, Inc. 552fa700-4215-d614-e063-6394a90aa12f 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Star Wars The Mandalorian and Grogu Force Flow ALCOHOL Bath & Body Works, Inc. 552fbaea-cc8f-ff08-e063-6294a90aa086 2026-06-26 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.