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GW501516 20 mg

PPAR-delta Agonist (Non-Hormonal Performance Enhancer)

Lab Tested

Substance: Cardarine (GW501516)
Strength: 20 mg/tablet
Form: Oral tablets
Packaging: 100 tablets / Sachet
Manufacturer: Dragon Pharma, Europe

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Dragon Pharma GW501516 (Cardarine)

Dragon Pharma GW501516 20 mg, widely known as Cardarine, is a revolutionary performance-enhancing compound that operates through a completely non-hormonal pathway. Unlike anabolic steroids or SARMs that work on androgen receptors, Cardarine is a potent PPAR-delta (Peroxisome Proliferator-Activated Receptor delta) agonist. This unique mechanism fundamentally changes how the body utilizes energy, shifting its primary fuel source from carbohydrates to stored fatty acids. The result is a dramatic and multifaceted enhancement of physical performance: drastically increased endurance, accelerated fat loss, and significant improvements in cardiovascular health markers.

Originally developed for metabolic and cardiovascular diseases, Cardarine's ability to enhance exercise capacity by up to 70% in animal studies made it a game-changer in the athletic world. Users report being able to train longer, harder, and recover faster between sets, making it invaluable for both cardio sessions and high-volume weight training. Furthermore, it actively improves blood lipid profiles by increasing HDL (good) cholesterol and decreasing LDL (bad) cholesterol and triglycerides, offering a protective effect often needed when using other performance-enhancing drugs. Dragon Pharma's 20 mg tablet, supplied in sachets of 100, provides an optimal dose for measurable results. It's important to note that while Cardarine is non-hormonal and non-suppressive, responsible use and adherence to recommended dosages are always advised.

Key Benefits:

Extreme Endurance & Stamina Boost: Dramatically increases cardiovascular endurance and work capacity, allowing for longer, more intense training sessions with reduced fatigue.
Enhanced Fat Burning & Metabolism: Switches the body's energy substrate to fatty acids, promoting efficient fat loss while preserving lean muscle mass, even in a calorie deficit.
Improved Cardiovascular Health: Positively impacts cholesterol by raising HDL and lowering LDL/triglycerides, offering cardioprotective benefits—a rarity among PEDs.
Faster Recovery: Reduces muscle damage and inflammation post-exercise, leading to quicker recovery between workouts.
Non-Hormonal & Non-Suppressive: Does not affect testosterone or other hormones, requires no Post Cycle Therapy (PCT), and can be used by both men and women.

Each sachet contains 100 tablets of 20 mg Cardarine (GW501516), manufactured under strict quality control standards in Dragon Pharma's certified facilities.

Product Specifications

Product Name	GW501516 20 mg
Manufacturer	Dragon Pharma
Substance	Cardarine (GW501516)
Packaging	100 Tablets / Sachet
Lab Test Result	21.70 mg (Exceeds label claim)
Half-Life	~16-24 hours
Recommended Cycle	8-12 weeks (with breaks)
Form	Oral Tablet
Aromatization	No (Non-hormonal)
Dosage	10 mg - 20 mg per day

Usage Guidelines

Important Note: While Cardarine is non-hormonal and well-tolerated, it is prudent to follow sensible cycle lengths and dosages. It is often used as a supportive compound alongside other agents.

Fat Loss & Endurance Cycle (8 weeks): 10 mg per day. Ideal for boosting cardio performance and accelerating fat loss. Can be stacked with a fat burner like Clenbuterol for synergistic effects.
Performance & Recomp Stack (10-12 weeks): 15-20 mg per day. For significant endurance gains and body recomposition. Commonly stacked with SARMs like MK-2866 (Ostarine) or LGD 4033 to build muscle while burning fat.
Cardiovascular & Lipid Support on Steroid Cycles (6-8 weeks): 10-20 mg per day. Used to mitigate the negative cholesterol impact of harsh orals like Anavar or Winstrol, while also improving endurance.

Post Cycle Therapy (PCT):

Cardarine does not require a traditional PCT as it is non-hormonal and does not suppress the HPTA. You can stop usage at the end of your cycle without a taper. Any PCT you run would be for other suppressive compounds in your stack, not for Cardarine itself.

Liver Protection & Health Support:

Cardarine is not methylated and is not known to be hepatotoxic. In fact, it may have protective effects.

Liver & Organ Health: No specific liver support is required for Cardarine alone. For general wellness on any cycle, consider support like TB-500/BPC-157.
Cardiovascular Synergy: Cardarine's primary health benefit is improving lipid profiles. To enhance this, maintain a heart-healthy diet rich in omega-3s.
Cycle Breaks: It is advisable to take breaks from Cardarine (e.g., 8 weeks on, 4-8 weeks off) to allow receptors to resensitize and as a general precautionary measure.

Third-Party Lab Tested

Dragon Pharma GW501516 20 mg (Cardarine) Lab Test Result June 2024

2024-06-18

View Result

21.70 mg

This independent lab analysis confirms Dragon Pharma GW501516 20 mg tablets contain 21.70 mg of active Cardarine, exceeding the labeled claim. This verifies not only authenticity but also consistent over-filling, ensuring you receive maximum potency and value for your endurance and cutting goals.

Storage Instructions

To preserve the chemical stability and potency of Cardarine tablets:

Store the sealed sachet in a cool, dry place away from direct light, heat, and moisture.
Optimal storage temperature is between 15°C and 25°C (59°F - 77°F).
Keep the tablets in their original, protective packaging until use.
Always keep out of reach of children and pets.
Do not use if the packaging is damaged or after the expiration date printed on the sachet.

Does Cardarine (GW501516) burn fat?

Yes, Cardarine is an effective fat-burning agent, but its mechanism is unique. It doesn't directly stimulate the nervous system like Clenbuterol. Instead, it activates PPAR-delta pathways, which reprogram metabolism to preferentially use stored fat as fuel during exercise and at rest. This shift in energy substrate utilization, combined with the dramatic increase in exercise capacity it provides, leads to significant fat loss over time, especially when paired with a proper diet and training regimen.

What is the mechanism of action of Cardarine?

Cardarine's mechanism is through agonism of the PPAR-delta (Peroxisome Proliferator-Activated Receptor delta) receptor. Activating this receptor triggers several effects: it increases the expression of genes involved in fatty acid oxidation (burning fat for energy), enhances glucose metabolism in muscles, and promotes the formation of "slow-twitch" endurance muscle fibers. Essentially, it tells the body to become more metabolically efficient, endurance-focused, and fat-adapted.

Does Cardarine change muscle fibers?

Yes, research indicates it can promote a shift toward more endurance-oriented muscle fibers. PPAR-delta activation encourages the development of Type I (slow-twitch) muscle fibers, which are more fatigue-resistant and efficient at using oxygen and fat for energy. This fiber-type shift is a key reason behind the massive endurance increases users experience. It does not directly build muscle size like an anabolic compound but changes the muscle's metabolic characteristics for better endurance performance.

Is Cardarine a SARM or a steroid?

No, Cardarine is neither a SARM nor a steroid. It is often grouped with SARMs for convenience but is pharmacologically distinct. SARMs selectively bind to androgen receptors. Cardarine does not interact with androgen or any sex hormone receptors at all. It is a PPAR-delta agonist, working on entirely different metabolic pathways. This is why it has no androgenic side effects and does not suppress natural testosterone production.

What are the cancer risks associated with Cardarine?

The cancer concerns stem from a now-famous rodent study where rats were given extremely high doses of Cardarine (equivalent to over 40 mg/day for a human) for almost their entire lifespan (2 years), leading to various cancers. It is critical to note: 1) Rodent metabolism differs significantly from humans. 2) The doses were massively supra-physiological. 3) The compound was given continuously for an extremely long time. Human equivalent doses (10-20 mg/day) for typical cycle lengths (8-12 weeks) have not been linked to cancer in humans. However, the potential risk is why users are advised to keep cycles reasonable and take breaks.

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