WHOLESALE PRODUCT SPECIFICATIONS
Lyophilized powder. White to off-white lyophilized powder. Compare presentations and review the available product documents before requesting a quote.
| Code | Presentation | Documents |
|---|---|---|
| TR10 | 10 mg x 10 vials | Request |
| TR15 | 15 mg x 10 vials | Request |
| TR20 | 20 mg x 10 vials | Request |
| TR30 | 30 mg x 10 vials | Request |
| TR40 | 40 mg x 10 vials | Request |
| TR60 | 60 mg x 10 vials | Request |
TR15 identifies the Tirzepatide 15 mg x 10 vials catalog presentation.
BATCH DOCUMENTATION
Request the COA matching your selected presentation and batch. Earlier submitted-sample reports and raw-material COAs, where available below, retain their own document scope.
No batch-linked finished-vial COA is currently published for this product.
Request the applicable document ↗These records retain their own sample or source-material scope and do not replace a matching batch COA.
TR20-20260917S8803 ·
Reported purity 99.79%, detected mass spectrum and net content 21.06 mg.
Applies only to the submitted TR20 vial sample. The report states that it is not CMA/CNAS certification and is not a legal certification document.
Open source PDF ↗024-T85-TSX ·
Vendor-issued raw-material COA reporting 99.03% HPLC purity and 93.9% peptide content.
Bulk source-material record only. It does not verify the finished TR20 sample or a future production lot.
Open source PDF ↗PRODUCT INFORMATION
WHOLESALE SOURCING
Yili lists six Tirzepatide presentations. The public TR20 finished-vial report applies only to its submitted sample; the bulk raw-material COA remains a separate evidence class.
Choose TR10, TR15, TR20, TR30, TR40 or TR60 and the number of ten-vial kits. A TR20 result does not establish the quality of another strength or future production lot.
State the TR code, first-order or repeat-order quantity and destination so availability can be checked against a real request.
Review TR20 and the raw-material document by their own identifiers and analytical scope.
Include label, carton, cap and document-link requirements only after the product and kit quantity are fixed.
Include the code, quantity, destination and batch or document number you want to review.
