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 48 of 158 · 3,155 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Everyone Hand Sanitizer Lavender Aloe ALCOHOL EO Products, LLC d15c1fb9-b25b-45b8-a119-ee4c86c8d91c 2026-03-03 Warnings Exact identifier unii: 3K9958V90M Advanced Hand Sanitizer ETHYL ALCOHOL Amazon.Com Services LLC 85421e9a-f1c9-4793-9479-8a072a610ed7 2026-03-03 Warnings, Adverse reactions Exact identifier unii: 3K9958V90M FOOTSPA PEDI ALCOHOL CHEMCO CORPORATION 3886a958-d035-ed15-e063-6294a90af1b5 2026-03-03 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Moisturizing Hand Sanitizer Starfruit Sangria ALCOHOL Bath & Body Works, Inc. 387caf6b-fda0-a63f-e063-6294a90a041a 2026-03-03 Warnings Exact identifier unii: 3K9958V90M Alcohol ALCOHOL Old East Main Co. 31a38e0e-41de-4638-9e86-df1923b64d52 2026-03-02 Warnings, Adverse reactions Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Lavender and Vanilla ALCOHOL Bath & Body Works, Inc. 29a37aad-c6d3-b174-e063-6394a90abc3e 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Lavender and Vanilla ALCOHOL Bath & Body Works, Inc. 38d5a11f-d0cb-30eb-e063-6394a90a6a49 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Lavender and Vanilla ALCOHOL Bath & Body Works, Inc. 2b0f3ca1-0a68-08a6-e063-6294a90a9df2 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Lavender and Vanilla ALCOHOL Bath & Body Works, Inc. 38e1c1d6-6511-4066-e063-6294a90ad3f4 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Ethyl Alcohol ETHYL ALCOHOL Old East Main Co. 479d5880-1e7e-481e-98df-dd98324d6ab8 2026-03-02 Warnings, Adverse reactions Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray White T Shirt ALCOHOL Bath & Body Works, Inc. 29a38d22-0685-37af-e063-6294a90a31e6 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Passionfruit and Banana Flower ALCOHOL Bath & Body Works, Inc. 38d5d6c2-8ceb-40b7-e063-6394a90a2a8f 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray A Thousand Wishes ALCOHOL Bath & Body Works, Inc. 29a3aac8-2083-3ece-e063-6394a90ab440 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Ocean ALCOHOL Bath & Body Works, Inc. 29a38d22-068a-37af-e063-6294a90a31e6 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Champagne Toast ALCOHOL Bath & Body Works, Inc. 29a3aa8a-c697-a873-e063-6294a90a72c4 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Peach Bellini ALCOHOL Bath & Body Works, Inc. 297e26d2-128e-0aa5-e063-6294a90a34dc 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Waikiki Beach Coconut ALCOHOL Bath & Body Works, Inc. 38d5cfd5-db0d-4735-e063-6394a90a42a8 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Sunshine and Lemons ALCOHOL Bath & Body Works, Inc. 297e95be-a862-9d13-e063-6294a90a9faa 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Sweet Kiwi and Starfruit ALCOHOL Bath & Body Works, Inc. 38d5d1c4-7f5b-45af-e063-6394a90a9c47 2026-03-02 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Ocean ALCOHOL Bath & Body Works, Inc. 38d5c6ac-4e71-3e9e-e063-6394a90af6c2 2026-03-02 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.