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 43 of 158 · 3,155 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti-BacterialHandSpray Winter Candy Apple ALCOHOL Bath & Body Works, Inc. 463f7ab4-e5f3-ab23-e063-6394a90a541b 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Marshmallow Pumpkin Latte ALCOHOL Bath & Body Works, Inc. 4650a56b-c159-b228-e063-6394a90a5a6e 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Bright Christmas Morning ALCOHOL Bath & Body Works, Inc. 4650bf54-c759-f503-e063-6294a90a1d2e 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Cookie Butter Truffle ALCOHOL Bath & Body Works, Inc. 468c92f6-9cae-0c6e-e063-6394a90a78ef 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Mrs. Claus Cocktail ALCOHOL Bath & Body Works, Inc. 468c93d1-8265-7cd2-e063-6294a90a5776 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Sparkling Snow ALCOHOL Bath & Body Works, Inc. 468c9682-6163-830f-e063-6294a90a76a9 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti-BacterialHandSpray White Tea and Sage ALCOHOL Bath & Body Works, Inc. 463fc2a9-742a-fbd3-e063-6394a90a0bf9 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Twisted Peppermint ALCOHOL Bath & Body Works, Inc. 4650b8b0-87be-8c88-e063-6394a90a52ed 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Cereal Milk Soft Serve ALCOHOL Bath & Body Works, Inc. 469140f3-24ed-88e5-e063-6394a90a2f51 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Peppermint Bark Truffle ALCOHOL Bath & Body Works, Inc. 469149e2-656a-cb52-e063-6294a90ad50c 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Apple ALCOHOL Bath & Body Works, Inc. 4650ae83-ed71-a7aa-e063-6294a90ad109 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 4650bbda-1646-da3a-e063-6294a90a67fa 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Blackberries and Basil ALCOHOL Bath & Body Works, Inc. 4650ab55-8ce4-a5e1-e063-6294a90a79bf 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Leaves ALCOHOL Bath & Body Works, Inc. 4650ae83-ed72-a7aa-e063-6294a90ad109 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Tis The Season ALCOHOL Bath & Body Works, Inc. 468c9ecb-1691-1e20-e063-6394a90a2e89 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberry Holiday Pie Bar ALCOHOL Bath & Body Works, Inc. 4691409f-30e6-799b-e063-6394a90a34cd 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Moisturizing Hand Sanitizer Snowy Peach Berry ALCOHOL Bath & Body Works, Inc. 4690a5fd-79cf-e1fd-e063-6294a90a009c 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Milk Bar Birthday Cake ALCOHOL Bath & Body Works, Inc. 469140f3-24ec-88e5-e063-6394a90a2f51 2026-03-10 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Apple ALCOHOL Bath & Body Works, Inc. 4690812f-0f94-a899-e063-6394a90af6b9 2026-03-10 Warnings Exact identifier unii: 3K9958V90M mild iodine tincture IODINE AND SODIUM IODINE AND ALCOHOL KROGER COMPANY 42762471-e5cb-505e-e063-6294a90afb7d 2026-03-10 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.