LO LOESTRIN FE

A-S Medication Solutions🇺🇸 United States

FDA Page

Effective Date: Feb 26, 2024
Approval ID: e2f24e91-4893-40bf-b310-d93db95d2442
Products: 1 registered
Version: 16

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use Lo Loestrin Fe safely and effectively. See full prescribing information for Lo Loestrin Fe. Lo Loestrin Fe (norethindrone acetate and ethinyl estradiol tablets, ethinyl estradiol tablets and ferrous fumarate tablets) Initial U.S. Approval: 1968

Quick Stats

Total Products1

Labelers2

Label Sections38

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.