Mirexa Mini

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)

Brand name: Mirexa Mini
Generic name: MIREXA MINI
Manufacturer: Oncora Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: ea48f64a-9a70-40df-ba25-098353273089
SPL ID: 7b6ff5fb-c082-43b1-836a-2430237e9fae
Version: 1
Effective date: 2026-08-25
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:45:41

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Mirexa Mini	openfda.brand_name
generic name		MIREXA MINI	openfda.generic_name
manufacturer name		Oncora Pharma, LLC	openfda.manufacturer_name
ndc	package	85477-925-30	openfda.package_ndc
ndc	product	85477-925	openfda.product_ndc
ndc11	package	85477092530	derived:openfda.package_ndc
spl id		7b6ff5fb-c082-43b1-836a-2430237e9fae	id
spl set id		ea48f64a-9a70-40df-ba25-098353273089	set_id
unii		R5L488RY0Q	openfda.unii
unii		935E97BOY8	openfda.unii
unii		PQ6CK8PD0R	openfda.unii
unii		81G40H8B0T	openfda.unii
unii		P6YC3EG204	openfda.unii
unii		1C6V77QF41	openfda.unii
unii		X66NSO3N35	openfda.unii

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Accidental overdose of iron-containing products is a leading cause of fatal poising in children under 6. KEEP THIS PRODUCT OUT OF REACH OF CHILDREN. In the case of accidental overdose, call a doctor or poison control center immediately.

Adverse reactions cross-check#

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folic acid. You should call your doctor for medical advice about serious adverse events. To reports adverse side effects or to obtain product information, contact Oncora Pharma at 888-321-2821.

Reported adverse events (FAERS/openFDA)#

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