Nylia 7/7/7

Aurobindo Pharma Limited🇺🇸 United States

FDA Page

Effective Date: Jul 1, 2022
Approval ID: 867c5630-51be-4469-bf79-6a5cd4302cfa
Products: 1 registered
Version: 8

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

Nylia 7/7/7 (Norethindrone and Ethinyl Estradiol Tablets USP) 0.5 mg/0.035 mg, 0.75 mg/0.035 mg and 1 mg/0.035 mg Rx only

Quick Stats

Total Products1

Labelers2

Label Sections16

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.