Lo-Zumandimine

Aurobindo Pharma Limited🇺🇸 United States

FDA Page

Effective Date: Oct 9, 2023
Approval ID: a8c718cc-e235-4710-a9e6-6c58433f3028
Products: 1 registered
Version: 9

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use LO-ZUMANDIMINE safely and effectively. See full prescribing information for LO-ZUMANDIMINE. LO-ZUMANDIMINE™ (drospirenone and ethinyl estradiol) tablets, for oral use Initial U.S. Approval: 2001

Quick Stats

Total Products1

Labelers2

Label Sections21

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.