MedPath

ZOOBY

Approved
Approval ID

bd49f704-4fc4-42a3-aa87-2b41d15d86bb

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 3, 2023

Manufacturers
FDA

Young Dental Manufacturing Co 1, LLC

DUNS: 006309355

Products 1

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

Sodium Fluoride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0273-0357
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateJanuary 3, 2023
FDA Product Classification

INGREDIENTS (1)

SODIUM FLUORIDEActive
Quantity: 2.72 g in 100 g
Code: 8ZYQ1474W7
Classification: ACTIM

MedPath

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

© 2025 MedPath, Inc. All rights reserved.

ZOOBY - FDA Drug Approval Details