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Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9

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Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9

Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9
Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9 Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9 Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9

Large Image :  Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9

Product Details:
Place of Origin: India
Brand Name: YUECUI
Certification: ISO9001
Model Number: Pharmaceutical grade. Slimming materials
Payment & Shipping Terms:
Minimum Order Quantity: 1KG-1000KG
Price: dollar 1KG $990 per kilogram $950 a kilo for more than 50 kilos
Packaging Details: 25KG 25 kilos a barrel
Delivery Time: 5-8
Payment Terms: Western Union, T/T, D/P, L/C
Supply Ability: 50000KG

Weight Loss Pharmaceutical Grade East Butramine Hydrochloride Slimming Drug CAS125494-59-9

Description
Name: Tombutrine Hydrochloride Appearance Trait: White Powder
Model Number: Pharmaceutical Grade Contact Information: WhatsApp+13148049998
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East Butramine Hydrochloride Slimming Drug

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Slimming Drug CAS125494-59-9

Weight Loss Drug Pharmaceutical Grade. Slimming Materials East Butramine Hydrochloride Slimming DrugCAS125494-59-9

Specification model: 98%

 

Properties: White or slightly white powder

 

This product is a central action obesity treatment. Its main mechanism is to inhibit the reuptake of norepinephrine, 5-hydroxytryptamine and dopamine and enhance satiety, but has no significant effect on the release of norepinephrine, 5-hydroxytryptamine and dopamine. < Pharmacokinetics > The average absorption rate of a single dose was 77%. The peak time of blood concentration was 1.2 hours. The oral clearance rate was 1750l/h, and the half-life was 11 hours. Through the hepatic first-pass effect, the cytochrome p450(3a4) isoenzymes of the liver are metabolized into pharmacologically active metabolites monodemethylated and dimethylated m1 and m2, and these activities are metabolized into pharmacologically active metabolites m5 and m6. The plasma concentrations of the drug form and its metabolites reached a peak within 3-4 hours after taking the drug, and the plasma concentrations of m1 and m2 reached a stable state within 4 days after taking the drug, and the concentration was twice as high as that of a single dose. Contraindications: ① patients with renal insufficiency ② hypertensive and diabetic patients usage and dosage: the recommended dose is 5-30mg once a day. If the weight loss is not significant for 2 weeks, the dosage can be increased to 40-500mg daily.

Contact Details
Zhejiang Yuecui Trading Co., Ltd

Contact Person: 张国庆

Tel: +861314804998

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