MedPath

EPST HOMO

DRUG FACTS:

Approved
Approval ID

8fa536b9-a2a2-4055-a09b-a10ce4546f61

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Apr 8, 2025

Manufacturers
FDA

Deseret Biologicals, Inc.

DUNS: 940741853

Products 1

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

Epstein-Barr Virus DNA, Epstein-Barr Virus Nosode

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code43742-2173
Product Classification
G
Generic Name
Epstein-Barr Virus DNA, Epstein-Barr Virus Nosode
Product Specifications
Route of AdministrationORAL
Effective DateApril 8, 2025
FDA Product Classification

INGREDIENTS (4)

WATERInactive
Code: 059QF0KO0R
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
HERRING SPERM DNAActive
Quantity: 15 [hp_C] in 1 mL
Code: 51FI676N6F
Classification: ACTIB
HUMAN HERPESVIRUS 4Active
Quantity: 15 [hp_C] in 1 mL
Code: 2A26YW7PNX
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

EPST HOMO - FDA Drug Approval Details