Tesamorelin COA

Tesamorelin — Certificate of Analysis

The information below summarizes analytical documentation associated with the identified sample or batch of Tesamorelin.

ANALYTICAL INFORMATION

• Compound: Tesamorelin
• Lot / Batch: TESA10-03112026
• Purity: 99.6%
• Identity: Confirmed — Tesamorelin
• Testing Method: Qualitative ID; Percent Purity; Quantitative Assay
• Laboratory: Analytical Formulations, Inc.
• Report Date: March 16, 2026
• Heavy Metals: <10 ppb — Pass
• Microbial Testing: TAMC 0 — Pass; TYMC 0 — Pass

BATCH-SPECIFIC DOCUMENTATION

Analytical results apply only to the sample or batch identified in the corresponding laboratory report. Results for one sample or batch should not be interpreted as results for a different sample or batch.

RESEARCH USE ONLY

This information is provided for laboratory research documentation purposes only. Testing documentation does not establish FDA approval, safety, efficacy, or suitability for human, veterinary, diagnostic, or therapeutic use.