Folixate

PureTek Corporation🇺🇸 United States

FDA Page

Effective Date: Dec 5, 2023
Approval ID: 0bb91f61-b61b-c894-e063-6394a90ae51c
Products: 1 registered
Version: 1

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

(Folic Acid, Vitamin D3 Tablet) Rx Only

Quick Stats

Total Products1

Labelers2

Label Sections10

Regulatory Agency

🇺🇸

U.S. Food and Drug Administration

United States

Data Sources & Disclaimer: Approval information is sourced from official FDA databases. This content is for informational purposes only and does not constitute medical or regulatory advice. Always refer to official FDA websites for the most current information.