NDC 86184-087-01 - ERTUGLIFLOZIN L-PYROGLUTAMIC ACID

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
86184-087
Requested NDC
86184-087-01
Package NDCs from labels
86184-087-01
Manufacturer
MAEDA INC
Effective date
2026-06-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ERTUGLIFLOZIN L-PYROGLUTAMIC ACID - MAEDA INCMAEDA INC2026-06-07BULK INGREDIENT - ANIMAL DRUG

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 1 of 1 ยท 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SEGLUROMETERTUGLIFLOZIN AND METFORMIN HYDROCHLORIDEMerck Sharp & Dohme LLCa6aeb99a-ce49-4125-90ce-642df3f1ebad2026-08-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: MLU731K321
STEGLATROERTUGLIFLOZINMerck Sharp & Dohme LLCe6f3e718-bb99-48f1-ab94-b9f0af05fed62026-06-03Warnings, Adverse reactionsExact identifier
unii: MLU731K321
STEGLUJANERTUGLIFLOZIN AND SITAGLIPTINMerck Sharp & Dohme LLCc2c553d8-5a9d-4366-bf53-8bdb5a876d192026-06-03Warnings, Adverse reactionsExact identifier
unii: MLU731K321

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.