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 44 of 158 · 3,155 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Advanced Alcohol Foaming Hand Sanitizer ETHYL ALCOHOL Betco Corporation LLC 0da8eb7f-2e14-a7d5-e063-6294a90a88e7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M KleenLine Essentials Foaming Hand Sanitizer ETHYL ALCOHOL Brady Industries 2969ce5b-39b4-47b7-e063-6394a90a1909 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Firecracker Pop ALCOHOL Bath & Body Works, Inc. 38e21dcc-ea88-c6cd-e063-6294a90a057e 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Eucalyptus and Spearmint ALCOHOL Bath & Body Works, Inc. 1a8f680b-ab3e-a550-e063-6394a90ac951 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Advanced ETHYL ALCOHOL Amazon.Com Services LLC f5722d72-96b5-4aea-a67a-68aeefb63203 2026-03-09 Warnings, Adverse reactions Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel In The Stars ALCOHOL Bath & Body Works, Inc. 1ab8735e-1481-040c-e063-6394a90aff9b 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Ocean ALCOHOL Bath & Body Works, Inc. 1ba6a47e-b5e2-eda2-e063-6294a90a0a68 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Black Cherry Merlot ALCOHOL Bath & Body Works, Inc. 1ba69e88-401b-2aa4-e063-6294a90a79d1 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Cozy Vanilla Almond ALCOHOL Bath & Body Works, Inc. 1ba6a804-b4b2-2b4c-e063-6294a90ac4f1 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Crisp Morning Air ALCOHOL Bath & Body Works, Inc. 1bba88b3-3d5b-ad96-e063-6294a90aa4f3 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sea and Sandstone ALCOHOL Bath & Body Works, Inc. 1bbaa2b3-9322-9aab-e063-6394a90a14c9 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel White Tea and Sage ALCOHOL Bath & Body Works, Inc. 1bba9834-3c88-f5af-e063-6394a90aa6bd 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pineapple Mango ALCOHOL Bath & Body Works, Inc. 38e09999-3473-2e4c-e063-6394a90a4b5d 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Mahogany Teakwood ALCOHOL Bath & Body Works, Inc. 1bba8dfa-947c-1ee2-e063-6294a90ae52a 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Strawberry Pound Cake ALCOHOL Bath & Body Works, Inc. 1bba8dfa-947f-1ee2-e063-6294a90ae52a 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel A Thousand Wishes ALCOHOL Bath & Body Works, Inc. 29a539bb-42e3-dc73-e063-6394a90a5fe9 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Peach Bellini ALCOHOL Bath & Body Works, Inc. 2b1124a3-9b14-07b6-e063-6394a90a4973 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Watermelon Lemonade ALCOHOL Bath & Body Works, Inc. 38e1bd3f-8e6e-7b68-e063-6394a90a8274 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sunshine and Lemons ALCOHOL Bath & Body Works, Inc. 1bba8dfa-9481-1ee2-e063-6294a90ae52a 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Midnight Blue Citrus ALCOHOL Bath & Body Works, Inc. 2b116b79-fe71-325a-e063-6394a90a045b 2026-03-09 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.