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 112 of 156 · 3,116 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti-BacterialHandSpray Sun Washed Citrus ALCOHOL Bath & Body Works, Inc. 29a3af85-35b5-80eb-e063-6294a90aadfd 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Cactus Blossom ALCOHOL Bath & Body Works, Inc. 29a39319-8d25-e86a-e063-6394a90a8a8c 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Boardwalk Vanilla Cone ALCOHOL Bath & Body Works, Inc. 29a3b5b3-c104-7754-e063-6294a90af8e7 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Sparkling Watermelon ALCOHOL Bath & Body Works, Inc. 29a3af99-8186-9ec6-e063-6294a90ab842 2024-12-19 Warnings Exact identifier unii: 3K9958V90M germstarONE ETHYL ALCOHOL Soaptronic, LLC a6909a0f-de15-51e3-e053-2995a90ab34f 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Vanilla Bean Noel ALCOHOL Bath & Body Works, Inc. 29a4f4f7-8ac5-383c-e063-6394a90ad2d5 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Frosted Coconut Snowball ALCOHOL Bath & Body Works, Inc. 29a4feca-c287-51cb-e063-6294a90a264a 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray Twisted Peppermint ALCOHOL Bath & Body Works, Inc. 29a4ff29-e2ee-526c-e063-6294a90ad01b 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Chiffon ALCOHOL Bath & Body Works, Inc. 29a539bb-42dd-dc73-e063-6394a90a5fe9 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel White Pumpkin ALCOHOL Bath & Body Works, Inc. 29a536a0-3fb9-c35f-e063-6394a90ae1e3 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Together Weather ALCOHOL Bath & Body Works, Inc. 29a534f2-46cd-ea47-e063-6394a90a1319 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Rose Water and Ivy ALCOHOL Bath & Body Works, Inc. 29a539bb-42e2-dc73-e063-6394a90a5fe9 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Vanilla Romance ALCOHOL Bath & Body Works, Inc. 29a540fd-60b5-eb1e-e063-6394a90a27f7 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Flannel ALCOHOL Bath & Body Works, Inc. 29a54361-e108-20d7-e063-6294a90a117a 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Frozen Lake ALCOHOL Bath & Body Works, Inc. 29a536d5-6abb-c0ef-e063-6394a90a15bb 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Marshmallow Pumpkin Latte ALCOHOL Bath & Body Works, Inc. 29a5342a-e6dc-ea55-e063-6394a90a11e8 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Apple ALCOHOL Bath & Body Works, Inc. 29a536d5-6abf-c0ef-e063-6394a90a15bb 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 29a54361-e107-20d7-e063-6294a90a117a 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Cupcake ALCOHOL Bath & Body Works, Inc. 29a53c91-0bda-f572-e063-6294a90ae895 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweater Weather ALCOHOL Bath & Body Works, Inc. 29a540fd-60b7-eb1e-e063-6394a90a27f7 2024-12-19 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.