Verification guide

How to verify your GLP-1 API source

Only semaglutide base is FDA-acceptable for compounding. Salt forms (sodium, acetate) are unapproved. Here's how to verify what API your provider uses.

Only semaglutide base is FDA-acceptable for compounding. Salt forms (sodium, acetate) are unapproved. Here's how to verify what API your provider uses.

About this article

Reviewed byDr. Samuel Lora, M.D.
RolePharmacology & Compounding Reviewer
First publishedMay 20, 2026
Last reviewedMay 20, 2026
Page typeIn-depth editorial guide
Sources15+ cited sources

Why this matters

The April 14, 2026 FDA action restricted unapproved salt forms of semaglutide (sodium, acetate). Only semaglutide base is the acceptable API. Providers using salt forms are operating outside FDA's framework.

Ask the provider directly

'What active ingredient form do you use for compounded semaglutide?' Acceptable answer: semaglutide base (USP-grade). Concerning answer: vagueness, 'proprietary,' or salt forms named.

Check the certificate of analysis

Reputable compounding pharmacies provide CoAs (Certificates of Analysis) showing potency, identification (HPLC), and purity testing. CoAs should reference the API form explicitly.

For NexLife specifically

NexLife publicly disclosed use of semaglutide base API following the April 14, 2026 FDA action. See our April 2026 FDA action analysis.