Wegovy® is an FDA-approved once-weekly injectable semaglutide pen manufactured by Novo Nordisk, FDA-approved in June 2021 for chronic weight management in adults with obesity or overweight with at least one weight-related comorbidity. The FDA-approved 2.4mg maintenance dose is administered following a structured dose-escalation schedule. Weight Method does not dispense or prescribe brand-name Wegovy®. Our prescribing providers issue patient-specific prescriptions for compounded semaglutide, dispensed by U.S.-licensed 503A compounding pharmacies. Compounded semaglutide is not FDA-approved.
From 2,000+ patients · Wegovy is already seeing results
Wegovy (semaglutide) is an FDA-approved GLP-1 medication for weight loss; in trials of the brand-name product, patients lost an average of 15-22% of their body weight. Weight Method does not dispense brand-name Wegovy — it offers compounded semaglutide, prescribed by licensed providers, from $199/month with virtual consultations and direct shipping.
Key Fact
Wegovy® (semaglutide 2.4mg) is FDA-approved for chronic weight management (June 2021), manufactured by Novo Nordisk. It is administered once weekly following a 16-20 week dose-escalation schedule to the 2.4mg maintenance dose. Weight Method's compounded semaglutide program is dispensed at $154/month and is not FDA-approved.
Source: FDA approval data — Wegovy® prescribing information
Wegovy (semaglutide 2.4mg) activates GLP-1 receptors in the brain to suppress hunger, reduce cravings, and slow digestion.
Wegovy works by activating GLP-1 receptors throughout the body, primarily in the brain's appetite-regulation centers. The semaglutide in Wegovy mimics the natural GLP-1 hormone, reducing hunger signals, increasing feelings of fullness, and decreasing food cravings -- including cravings for high-fat and high-sugar foods. It also slows gastric emptying to extend satiety after meals. Wegovy is dosed to a 2.4mg maintenance level, which is higher than the diabetes-focused dosing used for Ozempic.
FDA-approved for chronic weight management (2021) and cardiovascular risk reduction (2024). The first semaglutide product with an explicit anti-obesity indication.
Wegovy is FDA-approved as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial BMI of 30 kg/m2 or greater (obesity) or 27 kg/m2 or greater (overweight) with at least one weight-related comorbidity such as hypertension, type 2 diabetes, or dyslipidemia. In March 2024, the FDA also approved Wegovy to reduce the risk of cardiovascular death, heart attack, and stroke in adults with cardiovascular disease and obesity or overweight, making it the first anti-obesity medication with a cardiovascular risk reduction indication.
Once-weekly injection, 2.4mg maintenance dose, 16-20 week dose escalation, manufactured by Novo Nordisk.
Wegovy is available in five dose strengths -- 0.25mg, 0.5mg, 1mg, 1.7mg, and 2.4mg -- following a structured 16-20 week dose-escalation schedule to the maintenance dose of 2.4mg once weekly. It is FDA-approved as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management, and also carries an FDA-approved indication to reduce the risk of major adverse cardiovascular events in adults with cardiovascular disease and obesity or overweight.
Wegovy delivers the highest approved semaglutide dose, plus a distinct FDA-approved cardiovascular risk reduction indication.
Wegovy® is FDA-approved specifically for chronic weight management in adults meeting the FDA-approved indication. Patients seeking the FDA-approved brand-name Wegovy® obtain it through a retail pharmacy on a prescription from their treating provider. Weight Method does not dispense or prescribe brand-name Wegovy®. For patients who, after consultation with a Weight Method provider, choose compounded semaglutide as part of a chronic-weight-management program, Weight Method dispenses compounded semaglutide through U.S.-licensed 503A compounding pharmacies at $154/month all-inclusive (medication, licensed-provider evaluation, ongoing provider access, dose management, and home shipping). Compounded semaglutide is not FDA-approved.
Compounded GLP-1 medications dispensed by U.S.-licensed 503A pharmacies.

Compounded semaglutide. Once-weekly subcutaneous injection.

Compounded tirzepatide. Dual-action GLP-1/GIP, once-weekly subcutaneous injection.
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