FDA-APPROVED
DelatestrylActive: Testosterone Enanthate
Quick reference: Typical clinical dosing: 50 to 200 mg IM every 7 to 14 days. Pharmacokinetics overlap closely with cypionate.
Fast facts
Active
Testosterone Enanthate
Maker
Endo Pharmaceuticals (originator) and generics
FDA Approval
1953
Half-life
~7 days (mean)
Form
Intramuscular injection, oil vehicle. Common strength: 200 mg/mL.
Indication
FDA-approved for replacement therapy in conditions associated with deficiency or absence of endogenous testosterone
Dose schedule
Typical clinical dosing: 50 to 200 mg IM every 7 to 14 days. Pharmacokinetics overlap closely with cypionate.
Recommended monitoring
Same monitoring panel as cypionate: trough TT, sensitive E2, hematocrit, PSA.
Clinical notes
Functionally interchangeable with testosterone cypionate at equivalent doses in most US protocols.
Controlled substance. Testosterone esters are Schedule III in the United States. A valid prescription from a DEA-registered prescriber is required. This page is research informational reference only.
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Frequently asked
What is the typical dose schedule for Delatestryl?
Typical clinical dosing: 50 to 200 mg IM every 7 to 14 days. Pharmacokinetics overlap closely with cypionate.
What is the half-life of Testosterone Enanthate?
Delatestryl has a half-life of approximately ~7 days (mean). Steady-state plasma levels are reached after roughly four to six half-lives of consistent dosing.
What monitoring labs are recommended on Delatestryl?
Same monitoring panel as cypionate: trough TT, sensitive E2, hematocrit, PSA.
Is Delatestryl the same as compounded testosterone enanthate?
Delatestryl is a finished FDA-approved drug product with consistent quality control. Compounded testosterone enanthate produced by 503A or 503B pharmacies contains the same active ester but is not held to identical manufacturing standards. Verify the Certificate of Analysis when using a compound.
Is Delatestryl a controlled substance?
Yes. Testosterone and its esters are Schedule III controlled substances in the United States. A valid prescription from a DEA-registered prescriber is required to obtain Delatestryl legally. State-level regulations may impose additional restrictions.
Related
For research informational use only. Not medical advice. Delatestryl is a registered trademark of Endo Pharmaceuticals (originator) and generics. Consult a qualified healthcare provider before any clinical decision. ASCEND, ascendpeptide.org