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Anadrol Inj Oxymetholone - Dragon Pharma

Dragon Pharma

Anadrol Inj Oxymetholone - Dragon Pharma

Injection · 50 mg/ml · 10 ml

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CompoundOxymetholone
ClassDHT-derived oral anabolic
Half-lifeAbout 8-9 hours
DetectionUp to 8 weeks (urine)
Liver toxicityHigh
Water retentionHigh
Here is the contradiction that defines oxymetholone: it is a DHT-derived compound that does not aromatise, yet it holds water more visibly than almost anything else in the range, and the reference literature attributes that to estrogen-like activity rather than to conversion into estradiol. The half-life shown is the value recorded in the references, where the exact elimination figure is described as not established; detection ranges differ by source, from about 8 weeks in review material to 2 months in reference tables, with a specific long-term metabolite present beyond two weeks. The dose figures used on this page are the oral references, matched against the 50 mg per ml label.
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Anadrol Inj Oxymetholone - Dragon Pharma
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Quality First

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Product Overview

Dragon Pharma Anadrol Inj is oxymetholone presented as an injectable liquid at 50 mg per ml. The compound is a 17-alpha-methylated anabolic derived from dihydrotestosterone, and in clinical practice it is best known as a stimulant of erythropoiesis in anaemia - the reason its red blood cell effect is documented rather than anecdotal. Bodybuilding use copies none of that medical logic: the compound is chosen for how fast the scale and the bar move. The tablet form sits in the same line as Oxymetholon 50 mg.

The puzzle worth understanding before using it is water. Oxymetholone does not aromatise, so the fluid it holds is not estradiol-driven in the usual way; the reference material explains the effect through direct estrogen-like activity or progestin-type activity. That matters practically, because an aromatase inhibitor does not work on oxymetholone water the way it works on testosterone water. What does move the needle is dose, cycle length and sodium management, together with blood pressure monitoring, since pressure and fluid rise together on this compound more than on Dianabol Inj at comparable doses.

The injectable route bypasses the stomach but not the 17-alpha-methyl group, so the high liver toxicity rating recorded for oxymetholone stays exactly where it is, and the 4-6 week limit on cycle length comes with it. Used at the front of a mass phase, the compound lifts strength and weight faster than anything else in the line; it is a poor fit for a deficit, and combining it with another alkylated oral simply doubles the same organ exposure. Sore joints that follow heavy training weeks are often covered by Deca 300 in the same cycle.

Dosage Protocol

Every milligram figure below comes from the tablet literature, because the source material for this page holds no injectable schedule that has been validated on its own. Where a number appears, the 50 mg per ml label is quoted next to it so the arithmetic stays visible.

Beginner 25-50 mg a day in the tablet data, 4-6 weeks; start at the lower boundary, since hepatic and estrogen-like effects both climb with the dose
Intermediate 50-75 mg a day in the tablet data, given as two administrations because the recorded half-life is roughly 8-9 hours, 4-6 weeks
Advanced Up to 100 mg a day in the tablet data, 4-6 weeks maximum; going above 100 mg is explicitly not advised, for liver and estrogen-like reasons
Female Not recommended; the virilization risk recorded for this compound is high, and the sources used for this card contain no confirmed female protocol
Administration Intramuscular injection; at 50 mg per ml a 25-50 mg reference dose corresponds to a fraction of a millilitre, which is arithmetic on the label rather than a validated injectable schedule; rotate sites and keep volumes low

Suggested Protocols

Three placements for a compound that belongs in a surplus; every pill below opens the matching Dragon Pharma product page.

Mass kickstart over a long ester
Anadrol Inj - 4 weeks at the front + Enantat 400 - 400-600 mg per week
12 weeks; the injectable oxymetholone covers the first four weeks only, then the ester carries the cycle; blood pressure checked weekly throughout
Off-season size, joints covered
Anadrol Inj - 4 weeks at the front + Deca 300 - 300-400 mg per week + Sustanon 270 - 500 mg per week
12 weeks; the fluid load is the highest of the three plans here, so sodium, pressure and body weight get tracked rather than estimated
Strength priority, tendon caution
10-12 weeks; strength climbs faster than connective tissue adapts, so load progression is deliberate rather than maximal

One placement this compound does not have is a cutting cycle. The fluid it holds is visible, it does not respond to an aromatase inhibitor the way testosterone-driven water does, and the 17-alpha-methyl group rules out long use. Users who want a dry oral phase reach for Anavar 50 instead.

What to Expect

  • Speed. Strength and body weight usually move by the end of the first or second week, faster than with any other compound in the injectable line.
  • Visible fluid. By week 2-4 the added weight includes a large water component, so the mirror shows size before it shows definition.
  • Red cell effect. Erythropoiesis is stimulated, which some users notice as better training endurance and recovery.
  • Appetite and mood. They improve for some users and worsen for others; neither response is a dosing guide.
  • Lipids and pressure. HDL falls, LDL rises, and blood pressure tends to track the fluid gain.
  • The ceiling. Four to six weeks is the maximum because of the alkylation; longer runs trade liver exposure for very little extra gain.
  • Post-block drop. Strength falls back somewhat when the compound stops, which is why the base ester and the diet have to be in place beforehand.

Side Effects and Management

The unusual part of this profile is that the largest cosmetic side effect - water - is not an aromatisation problem and needs a different answer.

Water retention and rising blood pressureDose control, sodium and fluid management, weekly pressure checks, short cycle. Marked and dose-dependent; an aromatase inhibitor does not solve this one because the compound does not aromatise.
Hepatic strain from 17-alpha-methylationLiver enzymes before and during, 4-6 week limit, stop on a rising trend. Dose-dependent.
Gynecomastia (rare but documented)Nolvadex if tissue change appears, with reassessment rather than escalation. Uncommon despite the absence of aromatisation, probably through direct estrogen-like action.
Lipid shift (HDL down, LDL up)Blood lipids, diet and cardio; the lever is how long the compound is run. Dose-dependent.
Raised hematocrit from erythropoiesisComplete blood count during the cycle, hydration, dose reduction; blood donation only under medical direction. Tied to the compound's documented red cell effect.
Suppression of endogenous testosteroneA SERM-based recovery plan; HCG where cycles run long. Expected.

Post-Cycle Therapy

Oxymetholone leaves the system quickly, so the hormonal recovery plan can start soon after the last administration.

OnsetRoughly 2-3 days past the final administration in the reference timing; the injectable route has no sourced interval, so the size of that gap is a judgement call rather than a fixed number
Option ANolvadex from day one: 40 mg daily through the opening week, then 20 mg daily to complete about a month
Option BClomid as a single four-week course at 50 mg a day
Short low-dose blocksA single SERM can carry the recovery on its own, but natural production shuts down at any dose that works, so the therapy is not skipped
Follow-upOnce the course ends: total testosterone, LH, FSH, estradiol, lipids, liver enzymes and a complete blood count, since the red cell effect and the hepatic effect both belong to this compound's record
The text on this page is provided as reference material for research and educational use and is not a medical document. Oxymetholone is described here as an injectable research-grade anabolic substance for laboratory and informational purposes, not as a medicine and not as a treatment for any condition, including the anaemia indication that appears in clinical labelling. Dose figures restate published reference data and are not a recommendation or a prescription. Nothing on this page is medical advice. Keep the product out of the reach of children and comply with the regulations in your country.
What is Oxymetholone (Anadrol) used for?
Medically it is used to stimulate red blood cell production in anaemia, which is why its effect on erythropoiesis is documented. In bodybuilding it is used for rapid mass and strength, almost always as a short block at the start of a cycle rather than as a base compound.
What is the difference between injectable and oral Anadrol?
The active substance is the same oxymetholone, and the tablet form is sold in this line as Oxymetholon 50 mg. The difference is delivery: the injection avoids the first pass through the stomach, while the oral route is absorbed and processed there. Neither route removes the 17-alpha-methyl group, so the liver warning is identical, and no separate pharmacokinetic figures for the injectable were found for this card.
Anadrol Inj dosage: how is 50 mg/ml used?
The dose references are oral - 25-50 mg per day for a beginner, 50-75 mg for an intermediate, up to 100 mg for an advanced user, always 4-6 weeks. At 50 mg per ml those milligram amounts correspond to fractions of a millilitre, and that conversion is taken from the label, not from a validated injectable protocol.
Why does Anadrol cause water retention if it does not aromatize?
Because the fluid effect is not produced by aromatisation. Oxymetholone is a DHT derivative that does not convert to estradiol, and the reference literature attributes its water retention to estrogen-like activity through direct action or to progestin-type activity. Practically, that is why an aromatase inhibitor does not clear this particular water and why dose, cycle length and sodium control are the levers that do.
Can Anadrol cause gynecomastia?
Rarely, but it is documented, which is surprising for a compound that does not aromatise. The likely explanation in the reference material is the same estrogen-like activity that drives the water retention. If sensitivity or a lump appears, Nolvadex is the usual response, and any persistent tissue change means stopping and reassessing.
Is Anadrol good for cutting?
No. It holds water more visibly than anything else in this range, so it hides the conditioning a cutting phase is meant to reveal, and the 4-6 week limit makes it useless for a long diet. A dry oral such as Anavar 50 is the sensible choice when the goal is a deficit.
How long does an Anadrol cycle last?
Four to six weeks. That ceiling comes from two directions at once: the 17-alpha-methylation and its liver load, and the fluid and pressure effect, which becomes harder to manage the longer it runs. Most plans put the compound in the first four weeks and keep the rest of the cycle on an injectable base.
Do you need PCT after Anadrol?
Yes. The compound suppresses endogenous testosterone, so recovery has to be planned. The reference count begins roughly 2-3 days past the final dose: Nolvadex at 40 mg every day of the first week and 20 mg every day for the rest of a month-long run, or Clomid at 50 mg every day for four weeks.

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