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Exametazime

Exametazime (HMPAO) (for the preparation of Tc99m Exametazime injection)

Approved
Approval ID

6ea1fd48-c649-4e05-856e-bb123ce40a3f

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 1, 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.

Exametazime

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code51808-214
Product Classification
G
Generic Name
Exametazime
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateNovember 28, 2012
FDA Product Classification

INGREDIENTS (3)

EXAMETAZIMEActive
Quantity: 1 mg in 1 1
Code: G29272NCKL
Classification: ACTIB
SODIUM CHLORIDEInactive
Quantity: 6.75 mg in 1 1
Code: 451W47IQ8X
Classification: IACT
STANNOUS CHLORIDEInactive
Quantity: 11.4 ug in 1 1
Code: 1BQV3749L5
Classification: IACT

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Exametazime - FDA Drug Approval Details