Aurovela Fe 1/20(Aurovela Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets USP and Ferrous Fumarate Tablets) Rx only)

Aurobindo Pharma Limited🇺🇸 United States

FDA Page

Effective Date: Nov 21, 2023
Approval ID: 83513d13-5352-4d86-9dfd-fd1e456087c0
Products: 1 registered
Version: 12

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

Aurovela Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets USP and Ferrous Fumarate Tablets) Rx only

Quick Stats

Total Products1

Labelers2

Label Sections15

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.