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I 123 Mini

I-123 Mini Caps Medical Professional Information Sheet

Approved
Approval ID

ba4a725e-ba46-427c-b309-a5ddc3c881ab

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

May 23, 2012

Manufacturers
FDA

AnazaoHealth Corporation

DUNS: 011038762

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

I 123 Mini

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code51808-102
Product Classification
G
Generic Name
I 123 Mini
Product Specifications
Route of AdministrationORAL
Effective DateDecember 2, 2012
FDA Product Classification

INGREDIENTS (2)

IODIDE ION I-123Active
Quantity: 10 mCi in 1 1
Code: 8YWR746RPQ
Classification: ACTIB
SODIUM PHOSPHATE, DIBASICInactive
Quantity: 100 mg in 1 1
Code: GR686LBA74
Classification: IACT

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I 123 Mini - FDA Drug Approval Details