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Androver 50mg/tab 100 Tabletten by Vermodje
High Concentration

Androver 50mg/tab 100 Tabletten by Vermodje

Androver is an oral Oxymetholone tablet formulated at 50 mg per unit across a 100-tablet supply, engineered by Vermodje SRL with post-cycle therapy planning as the governing framework for safe and structured use. Each tablet delivers the full reference androgenic dose as a single analytically verified unit, making it straightforward to calculate cumulative exposure before PCT begins. Androver's release specification is validated through per-batch HPLC content-uniformity assay and LAL endotoxin screening at Vermodje's Chișinău facility — a compound-specific quality architecture applied independently to the tablet compression line.

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  • Delivers a full 50 mg dose per tablet with no splitting or approximation required for PCT-mapped cycle planning.
  • 100-tablet pack provides sufficient supply depth to complete a defined cycle plus retain documented end-date clarity for PCT onset.
  • HPLC content-uniformity verification at Vermodje's Chișinău facility confirms that cumulative exposure calculations used in PCT planning are based on accurate per-tablet API content.
  • Oxymetholone's rapid plasma clearance — within approximately 36–45 hours — allows PCT to begin almost immediately after the final dose, shortening the suppression window.
  • LAL endotoxin screening on incoming API ensures that the tablet matrix introduces no contaminating variables that could confound post-cycle liver enzyme interpretation.
  • Compact tablet form allows straightforward counting throughout the cycle, enabling precise identification of the final-dose day and PCT start date.

Key takeaways

  • Start PCT within 48 hours of the final Androver dose.
  • Use SERM agents — Tamoxifen or Clomiphene — to restart LH and FSH production.
  • Confirm HPG axis recovery with serial serum assay at PCT weeks two and four.
  • Calculate total cycle milligrams using the exact 50 mg per tablet concentration.
  • Monitor ALT and AST through the full PCT window, not only during the cycle.

Androver and Post-Cycle Therapy: The Recovery Framework Every User Must Plan Before Cycle Onset

Androver by Vermodje delivers Oxymetholone at 50 mg per tablet across a 100-unit pack, and its correct use is inseparable from a structured post-cycle therapy plan established before the first tablet is taken. PCT is the pharmacological bridge between the end of exogenous androgen exposure and the restoration of endogenous hypothalamic-pituitary-gonadal (HPG) axis function. Oxymetholone suppresses gonadotropin release — LH and FSH — through negative feedback at the hypothalamus and pituitary, a suppression documented by serum assay within the first two weeks of administration at 50 mg per day.

When to Begin PCT and Which Agents Apply

PCT timing is determined by the compound's elimination profile: because Oxymetholone clears the plasma within approximately 36–45 hours of the final dose based on its known half-life, PCT agents can be introduced within 24–48 hours of the last Androver tablet rather than the multi-week delay required after long-ester injectables. Selective oestrogen receptor modulators (SERMs) — primarily Tamoxifen at 20–40 mg per day and Clomiphene at 50 mg per day — are the evidence-supported pharmacological tools for restarting gonadotropin pulsatility, acting at the pituitary to displace negative feedback and restore FSH and LH secretion. Compared to aromatase inhibitor monotherapy used for the same purpose, SERM-based PCT produces faster measurable LH pulse recovery as assessed by serial serum assay.

Duration, Monitoring, and the Role of Bloodwork

Androver's 100-tablet count supports a complete structured cycle — including a conservative induction phase and a defined exit point — that maps directly to a four-to-six-week SERM-based recovery window. Recovery duration is not fixed: serum testosterone, LH, FSH, and ALT/AST panels drawn at week two and week four of PCT determine whether the HPG axis is recovering on trajectory or whether the SERM protocol requires extension. Vermodje's per-batch HPLC content verification means each 50 mg Androver tablet delivers a precisely accounted androgenic load, making cumulative exposure calculable and PCT onset plannable without approximation. Users must not skip the post-PCT bloodwork draw, as residual hepatic enzyme elevation — measured by ALT and AST — can persist beyond clinical symptoms and requires confirmation of normalisation before subsequent cycles are considered.

Usage

  1. Before taking the first tablet, establish baseline bloodwork: serum testosterone, LH, FSH, ALT, and AST. These values form the reference against which PCT efficacy will be measured.
  2. Take each 50 mg Androver tablet orally with water, ideally with a small meal to support gastric tolerance, and log the date of every dose to maintain an accurate cumulative milligram record.
  3. At week two of the cycle, repeat ALT and AST panels; use results to confirm hepatic tolerance before continuing and to update your cumulative exposure calculation.
  4. Identify your final-dose day in advance — before starting — so PCT agents (Tamoxifen or Clomiphene) are sourced and on hand before you need them; do not plan PCT retroactively.
  5. Take the last Androver tablet and begin PCT within 24–48 hours; the short elimination window of Oxymetholone makes delayed PCT start a missed recovery window, not a conservative choice.
  6. Draw a full panel — testosterone, LH, FSH, ALT, AST — at PCT weeks two and four to confirm HPG axis recovery is on trajectory; extend SERM therapy by two additional weeks if LH and FSH remain suppressed at the week-four draw.

Warnings

Contraindications: Androver is contraindicated in individuals with active hepatic disease, elevated bilirubin, prostate or breast carcinoma, pregnancy, and known hypersensitivity to Oxymetholone or any excipient in the tablet matrix. Do not use if baseline ALT or AST exceeds twice the upper reference limit before cycle onset.

Side Effects: Hepatotoxicity is the primary risk: ALT and AST elevation is expected and requires monitoring rather than tolerance. Additional effects include haematocrit increase, HDL suppression, LDL elevation, oedema, and HPG axis suppression that persists into the post-cycle window and is the direct rationale for structured SERM-based PCT.

Monitoring: Obtain liver enzyme panels (ALT, AST, bilirubin) and a full lipid profile at baseline, cycle week two, and within one week of the final dose. Repeat the panel at PCT week four to confirm hepatic normalisation. Any ALT or AST reading exceeding three times the upper reference limit during the cycle requires immediate cessation rather than dose adjustment.

PCT: Structured SERM-based PCT is mandatory after every Androver cycle. Tamoxifen at 20–40 mg per day or Clomiphene at 50 mg per day for a minimum of four weeks represents the evidence-supported standard. Serum testosterone, LH, and FSH confirmation of HPG recovery is required before concluding PCT; do not terminate SERM therapy based on subjective wellbeing alone.

Frequently asked questions

How soon after the last Androver tablet should post-cycle therapy begin?
PCT can begin within 24–48 hours of the final Androver dose. Because Oxymetholone's plasma elimination is complete within approximately 36–45 hours, SERM agents such as Tamoxifen or Clomiphene can be introduced almost immediately — unlike long-ester injectables that require a multi-week washout delay before gonadotropin-stimulating therapy becomes pharmacologically rational.
Which PCT medications are considered evidence-supported after an Oxymetholone cycle?
SERMs — specifically Tamoxifen at 20–40 mg per day and Clomiphene at 50 mg per day — are the primary evidence-supported options. Both act at the pituitary to displace negative feedback and restore LH and FSH secretion. hCG may be introduced during the final cycle week to prime Leydig cell responsiveness before the SERM phase begins, particularly after cycles exceeding four weeks.
How long does HPG axis recovery typically take after stopping Androver?
HPG axis recovery duration varies by individual exposure history, but most users see measurable LH and FSH recovery within four to six weeks of structured SERM-based PCT, confirmed by serial serum assay. Cycle length and total cumulative milligrams of Oxymetholone consumed are the two strongest predictors of recovery timeline; longer or higher-dose cycles extend the suppression window and may require extended PCT.
Does the 50 mg per tablet concentration of Androver make it easier to plan PCT timing?
Yes — at 50 mg per tablet, the highest single-unit concentration in this compound's product group, each dose is a precisely defined androgenic increment with no splitting required. This makes it straightforward to calculate total cumulative milligrams consumed across the cycle, which directly informs PCT onset timing and SERM dose selection based on the depth and duration of HPG suppression anticipated.
Can Androver tablets be stored and counted accurately across a full cycle and PCT planning period?
The 100-tablet jar format allows straightforward tablet counting throughout the cycle, giving the user a real-time visual of remaining supply and making it easy to set a firm end date before PCT begins. Tablets should be stored at room temperature away from moisture and direct light; Vermodje's blister-sealed production process maintains API stability through the declared shelf life, so tablets remain within specification when stored correctly. (2) angle_used

Manufacturer

Vermodje SRL's international presence reflects a deliberate expansion strategy that places Androver and the broader oral tablet range in distributor networks across European, Baltic, and select non-European markets. Unlike manufacturers who concentrate distribution within a single regional tier, Vermodje's Chișinău-based production facility operates at a scale where documented batch traceability — HPLC content assay, LAL endotoxin screening, and fill-weight uniformity data — travels with each lot through the distribution chain to destination markets. This traceability infrastructure supports the regulatory documentation requirements that international wholesale and pharmacy-adjacent distribution channels impose, giving distributors in multiple jurisdictions a verifiable quality record rather than a certificate of conformity alone. Vermodje's approach to regional availability is product-differentiated: Androver's 100-tablet oral format serves markets where oral androgenic compounds represent the primary accessible product category, and the pack size is calibrated to distribution logistics in those markets.

Product details

BrandVermodje
Active ingredientoxymetholone
Also known asAnadrol, Anapolon, Oxymetholone, Androver, Vermodje Anadrol
Strength50 mg
FormTabletten
Pack size100 pieces
Item numberORA-OXYM-VER-022

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