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Xeno Laboratories

Halotestin Fluoxymesterone Tablets - Xeno Laboratories

Oral · 10 mg/tab · 50 tabs

Out of stock
CompoundFluoxymesterone
ClassDHT-derived oral
Half-lifeAbout 9 hours
DetectionUp to 2 months
Liver toxicityHigh
Water retentionNone
A methylated oral built for top-end force rather than size, with a reference half-life close to nine hours, which is why the daily amount is split across several intakes. Nothing in it aromatizes, so fluid and chest tissue are not the concern; hepatic strain and the lipid shift are. Reference detection figures disagree, from a few days up to two months.
Halotestin Fluoxymesterone Tablets - Xeno Laboratories
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Quality First

All products are manufactured under strict quality standards and independently tested before release. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.

Halotestin is Xeno Laboratories' fluoxymesterone, a methylated oral anabolic sold as tablets. Its reputation runs ahead of its numbers: it is discussed as the strongest oral for raw force, and almost nobody buys it to add size.

That reputation holds because the compound does one job well. A short block lifts top-end strength without moving scale weight, and the absence of any aromatisation step keeps fluid and chest tissue out of the picture. Everything difficult about it comes from the methyl group rather than from the hormone.

Product Overview

Fluoxymesterone is a 17-alpha-alkylated steroid built on a DHT backbone, the family that cannot be converted to estradiol at any dose. The methyl group at carbon 17 is what lets the tablet survive first-pass metabolism, and it is also why the hepatic load is classed as high. Reference figures put the half-life near nine hours, short enough that one daily tablet leaves obvious gaps and long enough that three or four smaller intakes hold a flatter level.

The clinical record is narrow. The drug was studied as replacement therapy at 5 to 20 mg a day and used palliatively at 10 to 40 mg a day, so athletic amounts sit in the same territory as medical ones. Competition use is strictly short-term: two to four weeks attached to an injectable base such as Xeno testosterone, where the tablets supply the strength edge and the oil does the tissue building.

What it will not do is add muscle. There is no fluid to shed and no dramatic weight shift to expect, so anyone shopping for a bulking oral has picked the wrong item in this line. Anadrol and Dbol 20 fill that slot; fluoxymesterone belongs elsewhere on the calendar.

Dosage Protocol

Published and vendor protocols stay in a narrow band, and the ceiling is not far above the floor.

Beginner 10 mg daily across 2-3 weeks, which already matches the top of clinical replacement dosing
Intermediate 10-20 mg daily across 2-4 weeks, split into three or four intakes
Advanced 20-30 mg daily across 2-4 weeks at most; no source describes a longer protocol
Female Not recommended; voice change and hair growth are the documented risks and no athletic female dose appears in the source material
Administration Oral, split across the day because of the short half-life

Dividing the amount matters more than the total. A single morning tablet leaves the afternoon uncovered, and smaller repeated intakes also smooth out the irritability that a large peak can bring. Because the amount used is small, tablet strength decides how the daily figure is assembled rather than how much hormone is actually taken.

Suggested Protocols

Three placements cover most real use. Every pill in the diagrams links to that product's page in this line.

Peak strength finish
Ten to twelve weeks on the injectable, with the tablets added for the last two or three weeks only
Dry contest prep
Four weeks is the ceiling, and never with a second methylated oral running at the same time
Single-oral strength block
Two to three weeks, then stop; hepatic enzymes are checked before any repeat

What to Expect

  • Drive and aggression inside days. Users describe a sharp, focused training state early in the block, usually before the weights on the bar have moved at all.
  • Force without scale movement. Working loads climb while body weight stays put, which is exactly why this is chosen over a wet oral.
  • A tighter, drier look. Subcutaneous fluid is not part of the profile, so definition and vascularity improve over the final fortnight.
  • A short window by design. Two to four weeks is the practical limit, and the strength at the end of that window is what the tablets were bought for.
  • Mood can shift. Patience and temper are the usually reported irritants, and they track dose rather than training.
  • Nothing is kept afterwards. The edge fades once the tablets stop, because the effect was neural and fluid-free rather than structural.

Side Effects and Management

The list is short, and the first two entries explain why the block is measured in weeks rather than months.

Raised liver enzymesEnzyme testing before, during and after, a fixed short block, and no second methylated oral in the same stack. The class effect of this oral.
Falling HDL and rising LDLLipid panel, dietary fat quality and aerobic work. Moves quickly at these amounts.
Irritability and aggressionKeep the amount at the lower end, split the intakes and stop early if mood becomes a problem. Common.
Acne, oily skin and scalp hair lossA consistent skin routine plus dose control; the DHT backbone makes these likelier in predisposed users.
Masculinising effects in womenDo not use. Voice lowering can be permanent even at low amounts.
Fluid retention and pressure changesRare but documented; check blood pressure if puffiness or headaches appear.

Post-Cycle Therapy

The tablets clear quickly, so timing is decided by the injectable underneath rather than by the oral.

When to startTwo days after the last tablet when nothing else was running; with a long ester base, wait for that ester to clear first
SERM routeTamox at 40 mg daily for seven days, then 20 mg daily for a further three weeks
AlternativeClomiphene at 50 mg daily across four weeks if the first option does not suit
Short blocksEven a two-week run suppresses production, so therapy is trimmed rather than omitted
BloodworkTotal and free testosterone, LH and FSH, estradiol, a lipid panel and hepatic enzymes once therapy ends
Published as educational and research reference material only. Nothing on this page is a prescription, a treatment recommendation or medical advice, and the compounds described are research-grade materials supplied for laboratory work rather than medicines. The dosing information reflects published clinical and vendor reference data for the active substance. Keep products away from children and comply with the regulations in force in your country.
What is Halotestin and what does fluoxymesterone do?
Halotestin is the trade name for fluoxymesterone, a 17-alpha-alkylated oral anabolic derived from DHT. It is taken for top-end strength and a harder look rather than for size, and it is normally attached to an injectable base for a short block of two to four weeks.
What amount is used for a strength phase?
Reference protocols sit between 10 and 30 mg a day, with beginners at the bottom and advanced users at the top. The material used for this page describes nothing above 30 mg daily, and medical use runs from 5 to 20 mg for replacement and 10 to 40 mg palliatively. Divided intakes through the day are standard.
Does Halotestin cause water retention or gynecomastia?
Aromatisation does not happen with this molecule, so water gain and chest tissue are not expected from the compound itself. Fluid retention and raised pressure do appear as rare listed reactions, and any chest symptoms should be reported rather than ignored.
How long should a Halotestin block run?
Two to four weeks is the practice described in the sources, and the limit comes from the liver rather than from tolerance or results. Longer runs have no support in the reference material, and stacking a second methylated oral at the same time shortens the safe window further.
Why does the liver need watching on this oral?
The 17-alpha-alkyl group is what lets the tablet survive the first pass through the liver, and the same feature puts strain on the organ. Enzyme values can rise noticeably at 10 to 20 mg a day, so testing before, during and after the block is the routine check, alongside the lipid panel that shifts the wrong way.
How long does Halotestin stay detectable?
Sources disagree here. One reference places urinary metabolites at up to five days after a single 10 mg tablet, while vendor profiles extend the window to about two months. The wide gap is a property of the published data rather than of the product, and no single figure should be treated as settled.
Do you need post-cycle therapy after Halotestin?
Yes. Natural production is suppressed at any effective amount, and a short block reduces the length of therapy rather than removing the need for it. Tamox at 40 mg daily for a week followed by 20 mg daily, or clomiphene at 50 mg daily for four weeks, with bloodwork once the protocol finishes, is the standard shape.
How do I verify a Xeno Labs supplier before ordering?
Ask for the batch number on the label of the Halotestin pack and check it against the vendor verification point before paying. Where a product has a verification route, the batch code is the only identifier that ties a specific pack to a supplier, so a seller who cannot produce one is describing stock it does not control.

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