Microgestin Fe

Physicians Total Care, Inc.🇺🇸 United States

FDA Page

Effective Date: Apr 26, 2012
Approval ID: 54262321-1af5-4433-88c6-4409ff428079
Products: 2 registered
Version: 1

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

MICROGESTIN 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets USP) MICROGESTIN Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets USP and Ferrous Fumarate Tablets*) *Ferrous fumarate tablets are not USP for dissolution and assay. MICROGESTIN 1.5/30 (Norethindrone Acetate and Ethinyl Estradiol Tablets USP) MICROGESTIN Fe 1.5/30 (Norethindrone Acetate and Ethinyl Estradiol Tablets USP and Ferrous Fumarate Tablets*) *Ferrous fumarate tablets are not USP for dissolution and assay. Rx only Revised: October 2007 14786

Quick Stats

Total Products2

Labelers2

Label Sections35

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.