Tadalafil (Cialis) -Male Enhacer Raws

Tadalafil (Cialis) Raw Steroid Powders CAS 171596-29-5 Sex Enhancement Medicine

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Tadalafil Description:
Tadalafil (INN) is a PDE5 inhibitor marketed in pill form for treating erectile dysfunction (ED) under the name Cialis see-al-iss, and under the name Adcirca ad-sur-kuh for the treatment of pulmonary arterial hypertension.
In October 2011 the U.S. Food and Drug Administration (FDA) approved Cialis for treating the signs and symptoms of benign prostatic hyperplasia (BPH) as well as a combination of BPH and erectile dysfunction when the conditions coincide. It initially was developed by the biotechnology company ICOS, and then again developed and marketed worldwide by Lilly ICOS, LLC, the joint venture of ICOS Corporation and Eli Lilly and Company. Cialis tablets, in 2.5 mg, 5 mg, 10 mg, and 20 mg doses, are yellow, film-coated, and almond-shaped. The approved dose for pulmonary arterial hypertension is 40 mg (two 20 mg tablets) once daily.

Tadalafil is also manufactured and sold under the name of Tadacip by the Indian pharmaceutical company Cipla in doses of 10 mg and 20 mg.

On November 21, 2003 the FDA approved tadalafil (as Cialis) for sale in the United States as the third ED prescription drug pill (after sildenafil (Viagra) and vardenafil (Levitra)). Like sildenafil and vardenafil, tadalafil is recommended as an 'as needed' medication. Cialis is the only one of the three that is also offered as a once-daily medication.

Moreover, tadalafil was approved in May 2009 in the United States for the treatment of pulmonary arterial hypertension and is under regulatory review in other regions for this condition. In late November 2008,

Tadalafil (Cialis) (Steroids) Spec.

CAS NO.: 171596-29-5
Alias:TADALAFIL(CIALIS);(cialis);Cialis/tadalafil;Cialis(IC351)
EINECS: 233-432-5
Assay: 99%
Molecular Formula:C22H19N3O4
Molecular Weight:389.341
Description: White Crystalline Powder
Storage: Shading, Confined Preservation
Package: as requirements or normal package