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 45 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 Warm Vanilla Sugar ALCOHOL Bath & Body Works, Inc. 38d6f6a0-52bf-df77-e063-6394a90a4464 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Crystal Blue Coast ALCOHOL Bath & Body Works, Inc. 38e1480e-d217-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberry Tangerine ALCOHOL Bath & Body Works, Inc. 38e1cc04-7905-74e4-e063-6394a90a7b4c 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Backyard Honeysuckle ALCOHOL Bath & Body Works, Inc. 38e1480e-d21c-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 38e1480e-d21d-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberries and Whipped Vanilla ALCOHOL Bath & Body Works, Inc. 38e1cef4-4814-745c-e063-6394a90aebf0 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fiji White Sands ALCOHOL Bath & Body Works, Inc. 38e1c1d6-6505-4066-e063-6294a90ad3f4 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweetest Song ALCOHOL Bath & Body Works, Inc. 38e1d907-75d7-3906-e063-6294a90a2ed7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Endless Weekend ALCOHOL Bath & Body Works, Inc. 38e15918-9ee2-4061-e063-6294a90a881c 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pina Colada Swirl ALCOHOL Bath & Body Works, Inc. 38e1e122-2087-90fa-e063-6394a90ab625 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Eucalyptus and Spearmint ALCOHOL Bath & Body Works, Inc. 38e1f8da-2003-80ba-e063-6394a90a2d1d 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweet Orange and Agave ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f10-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Book Loft ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f11-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Turquoise Waters ALCOHOL Bath & Body Works, Inc. 38e1d9e9-08e7-3908-e063-6294a90adf6b 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sunlit Palm Trees ALCOHOL Bath & Body Works, Inc. 38e1d907-75d0-3906-e063-6294a90a2ed7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Watermelon ALCOHOL Bath & Body Works, Inc. 38e1f4cd-7707-404a-e063-6294a90afc92 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Pineapple Sunrise ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f12-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Beach Weather ALCOHOL Bath & Body Works, Inc. 38e1dc79-bdc3-3b84-e063-6294a90a61d7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Amalfi Lemon ALCOHOL Bath & Body Works, Inc. 38e1f158-187c-3b86-e063-6294a90a396f 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Peach Blossom ALCOHOL Bath & Body Works, Inc. 38e1d907-75d9-3906-e063-6294a90a2ed7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.