BETIATIDE - Food and Drug Administration

Manufacturer: Food and Drug Administration
Effective date: 2020-06-17
Label type: Indexing - product concept
Version: 2
Source: full-release
Hydrated at: 2026-06-05 00:19:03

Label at a glance#

ProductBETIATIDE

Active ingredientBETIATIDE

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

BETIATIDE

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BETIATIDE	9NV2SR34P8	ACTIB

Source Document#

Source XML

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Kit for the Preparation of Technetium Tc99m Mertiatide	BETIATIDE	Sun Pharmaceutical Industries, Inc.	0ad62039-f848-4f3d-b489-2524e6b6b86e	2024-09-10	Warnings, Adverse reactions	Name fallback generic name: BETIATIDE

Reported adverse events (FAERS/openFDA)#

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