FDA label 34e51e9d-9076-4013-b800-33276a1a1a89

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID: 4f98b4a9-cc50-4386-98ef-6fb19d8e2abd
SPL ID: 34e51e9d-9076-4013-b800-33276a1a1a89
Version: 2
Effective date: 2013-04-04
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:59:35

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		34e51e9d-9076-4013-b800-33276a1a1a89	id
spl set id		4f98b4a9-cc50-4386-98ef-6fb19d8e2abd	set_id

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

Warnings: If symptoms persist or worsen, consult a healthcare professional

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