FDA Advisory No.2023-1813 || Certification of Contraceptive Products in Compliance to the Implementing Rules and Regulations of the Republic Act No. 10354, Also Known as the Responsible Parenthood and Reproductive Health Act of 2012

In compliance with Republic Act No. 10354, also known as “The Responsible Parenthood and Reproductive Health (RH) Act of 2012” and its IRR, the Food and Drug Administration (FDA) hereby invites all interested parties to submit position papers and any corresponding evidences on submitted non-abortifacient property evidence of the applicant below within ten (10) working days from the posting of this Advisory:  

 

Generic Name	Dosage Strength and Form	Brand Name	Applicant
Levonorgestrel	75 mg Subdermal Implant	Levoplant	DKT Health, Inc.

 

Position papers, documents and scientific evidence can be submitted via email to the Food and Drug Action Center (FDAC) [email protected] on Mondays to Fridays, 8:00 AM to 5:00 PM.