Dragon Pharma

Superdrol Inj Methyldrostanolone - Dragon Pharma

Name: Superdrol Inj Methyldrostanolone - Dragon Pharma
Brand: Dragon Pharma
SKU: OFFER-4918
Price: 95.0 USD
Availability: InStock

Injection · 40 mg/ml · 10 ml

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CompoundMethyldrostanolone

ClassDHT-derived 17-alpha-alkylated

Half-lifeShort (unconfirmed)

Detection3-10 days (up to 11)

Liver toxicityHigh

Water retentionNone

This is the driest compound in the Dragon Pharma injectable range and also the harshest on the liver. The molecule is 17-alpha-alkylated, so the injection route does not soften the hepatic profile - clinical reports describe cholestatic jaundice and liver injury even on short courses. Nothing here aromatises, so water retention and gynecomastia are not part of the picture; the price is joint dryness and a flat, low-estrogen feel at cycle doses. The exact half-life figure is not confirmed in any source used here, which is why the dosing interval is stated as short rather than given a number.

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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.

Product Overview

Dragon Pharma Superdrol Inj is methyldrostanolone, better known as methasterone or Superdrol, presented as an injectable solution at 40 mg per ml. The compound is a 2-alpha,17-alpha-dimethyl derivative of dihydrotestosterone, which places it at the dry end of the alkylated range: no aromatisation, no water, and a hepatic profile that the medical literature treats as its defining problem. The brand also lists the same substance as tablets in Superdrol 10 mg for users who prefer the oral route.

The injectable format is unusual for this compound and it is worth being clear about what it does and does not do. It does put the substance into circulation without a first pass through the stomach, which keeps the dose away from the digestive tract. It does not change the molecule: the 17-alpha-methyl group is still there, and published case reports describe cholestatic jaundice and liver damage after short courses of methasterone, including courses of a few weeks. That is why the liver lines in the table below are not a precaution written for legal reasons - they are the documented profile of this substance.

What the compound is used for is narrow and specific: a short block of dry size and strength at the front of a cycle, without the water that comes with a wet oral such as Dianabol Inj or Anadrol Inj. Because it does not aromatise, the base underneath the block has to come from elsewhere, and a testosterone ester is the standard source. Users chasing a dry look pair it with a low-water base and keep the block to three or four weeks.

Dosage Protocol

The dose references in the fact base for this compound are oral, and the fact base does not record a validated injectable protocol. The milligram figures below are those references, with the label concentration of 40 mg per ml noted for conversion.

Beginner	10 mg per day in the oral references, 3 weeks; at 40 mg per ml that dose is a quarter of a millilitre, a conversion taken from the label rather than from a sourced injectable schedule
Intermediate	10-20 mg per day in the oral references, 3-4 weeks, split into two administrations because the half-life is short
Advanced	Up to 30 mg per day in the oral references, never beyond 4 weeks; above that figure complaints about the liver rise sharply, and the ceiling is a warning, not a goal
Female	No confirmed protocol exists for women on this compound, and the virilization risk of a DHT-derived anabolic is not something the sources treat as manageable at any dose
Administration	Intramuscular injection; the exact elimination half-life is not confirmed in the sources used here, so the interval between injections is not fixed by a sourced figure and the split-dose logic follows the tablet data

Suggested Protocols

The blocks below are short by design. In each case the alkylated compound opens the cycle and stops; the injectable base is what the cycle is actually built on.

Three-week dry block

Superdrol Inj - 3 weeks only + Enantat 250 - 350-500 mg per week

12 weeks total; aromatase control applies to the testosterone base, never to the Superdrol block itself

Recomposition at low body fat

Superdrol Inj - 3 weeks only + Masteron 100 - 300 mg per week + Cypionat 250 - 250 mg per week

10-12 weeks; the cosmetic difference comes from body fat and diet, and the dry compounds only remove the water layer on top

Strength block, wet orals avoided

Superdrol Inj - 3 weeks only + Sustanon 270 - 500 mg per week + HCG 5000 iu - during the cycle

10 weeks; chosen instead of a Dianabol or Anadrol kickstart when water and blood pressure are the concern

One rule sits outside the cards: this compound is alkylated, so combining it with any other alkylated oral stacks the same organ risk twice. Methyl-1-Test and Halotestin are the compounds to keep out of the same plan.

What to Expect

Strength first. Users typically report force output and muscle density changing within days rather than weeks, which is exactly why the block is measured in weeks.
Dry weight. Gains look hard because nothing is stored as subcutaneous water; there is no puffiness to hide a soft condition.
No gynecomastia pathway. The compound does not aromatise, so breast tissue changes are not expected from it alone - the base compound is the usual source of that risk.
Joints and mood. Dry joints, aching and a flat, unmotivated feeling are common complaints, driven by very low estrogen and a suppressed axis.
Liver enzymes. A rise in ALT, AST and bilirubin is expected on this compound and is the reason for the short block and the lab work.
Axis shutdown. Suppression is strong even on a three-week course, so recovery is planned rather than assumed.
Limit of the tool. The published liver-injury cases are part of the molecule profile; no dose schedule makes that risk disappear.

Side Effects and Management

Two features define the side effect profile: no estrogenic activity at all, and a liver risk documented in clinical case reports.

Rising liver enzymes, signs of cholestasisALT, AST and bilirubin before and during the block; stop on a rising trend instead of pushing through it. Frequent and dose-dependent, with hepatic injury reported even on short courses.

Lipid shift (HDL collapse)Lipid panel, diet and cardio; a three-week exposure is the main lever available. Frequent and dose-dependent.

Blood pressure increaseHome monitoring, dose reduction or stopping if pressure climbs. Frequent.

Dry joints and achingLower training volume on heavy compounds, hydration, and reconsideration of the dose. Frequent.

Lethargy and low moodA consequence of near-zero estrogen and a suppressed axis; post-cycle therapy is the fix, and stopping early is the answer if it is pronounced. Frequent on cycle.

Virilization in womenImmediate discontinuation at the first sign; no confirmed female protocol exists for this compound.

Post-Cycle Therapy

The compound is gone quickly, but the suppression it leaves behind is not, so therapy starts early in either case.

OnsetOne day after the last oral dose in the reference timing for this compound; for the injectable product the interval follows the ester and carrier of the format, which the sources for this card do not specify

Option ANolvadex in a step-down pattern: weeks 1-2 at 40 mg a day, weeks 3 onward at 20 mg a day for a further two to four weeks

Option BClomid at 50 mg a day: four weeks is the floor and six the ceiling of the recorded window

Short low-dose blocksSuppression is strong even after three weeks, so the short length of the cycle is not an argument for skipping therapy

Follow-upDraw the panel 4-6 weeks after therapy closes: LH, FSH, estradiol and total testosterone, together with ALT, AST, bilirubin and a lipid profile. On this compound the liver values deserve as much attention as the hormonal ones

This card is reference material for research and educational reading, not a medical document. The substance is described as an injectable research-grade anabolic item for laboratory and informational purposes; it is not presented as a medicine, a prescription or a treatment for any condition, and the milligram figures reproduce published reference data rather than a recommendation. Clinical reports of liver injury with this compound are referenced because they are part of its record. Nothing here is medical advice. Keep it away from children and respect the law where you live.

What is Superdrol Inj (methyldrostanolone)?

It is Dragon Pharma methyldrostanolone, also called methasterone, in a 40 mg per ml injectable solution. The compound is a dimethylated dihydrotestosterone derivative sold as a designer anabolic from 2005 until regulators moved against it. It does not aromatise, so it produces no water weight, and its hepatic profile is the harshest in the range.

Is Dragon Pharma Superdrol legit or are there fake batches around?

Counterfeits of popular injectables exist in every market, and Superdrol is a compound that is easy to fake because the expected effect is fast and subjective. Practical checks are the same for all injectables: intact crimp and stopper, legible label with a lot number, no particles or cloudiness in the solution, and consistency of the vial across a batch. Brand reputation discussions on forums are not verification - a laboratory analysis of the lot is the only real one.

Superdrol dosage - how much and how long?

The recorded references are oral: 10 mg per day for a first course, 10-20 mg per day for an experienced user and up to 30 mg never beyond four weeks. On a 40 mg per ml label a 10 mg dose is a quarter of a millilitre, but that is a conversion from the label, not a validated injectable protocol. Above 20 mg per day the reports of liver trouble increase sharply.

Run Superdrol for 2 or 3 weeks?

Three weeks is the common first block and four weeks is the outer edge in the reference ranges. Two weeks is shorter than what the data describe but is a defensible stopping point if liver markers move early. The right decision rule is the blood test, not the calendar: when ALT and bilirubin climb, the block is over.

Why is Superdrol so liver toxic?

Because of the 17-alpha-methyl group that lets the molecule survive oral administration. Methasterone belongs to the category of compounds that the literature labels as hepatotoxic, and published case reports describe cholestatic jaundice and liver damage after short courses. Injecting bypasses the digestive tract but leaves the methyl group in place, so it does not remove the risk.

Does Superdrol cause water retention or gyno?

No to both, from this compound alone. It is a DHT derivative that does not aromatise, so no estradiol is produced and no subcutaneous water is stored; gynecomastia is atypical for that reason. If breast tissue changes appear during a cycle containing a testosterone base such as Enantat 250, the base is the likely cause.

How long does Superdrol stay in your system for a drug test?

Metabolites of methasterone are usually detectable in urine for about 3-10 days, with some published work reporting up to 11 days. That is short compared with long esters, but it is long enough that a test taken in the days after a block can still find them. The substance is on the WADA prohibited list as an anabolic agent.

Do you need PCT after Superdrol, and when do you start it?

Yes. Three weeks of this compound suppresses the axis hard, so recovery is not optional. The reference start is the day after the last oral dose and the injectable interval depends on the ester in the format, which the sources here do not state. The standard routes are Nolvadex stepped down from 40 mg a day to 20 mg a day and held there for two to four weeks, or Clomid at 50 mg a day for four to six weeks.

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