Pharmaceutical Levetiracetam Sodium Capsule Purity Levetiracetam Powder Material Levetiracetam

• Powder: Yes
• Customized: Customized
• Certification: GMP, HSE, ISO 9001, USP, BP
• Suitable for: Elderly, Children, Adult
• State: Powder
• Purity: >99%
• Model NO.: D-sung Levetiracetam
• Product Name: Levetiracetam
• Name: Levetiracetam Powder
• Appearance: White Powder
• Color: White
• Grade: Pharmaceutical Grade
• Assay: HPLC 99%
• Application: Pharmaceutical;Anti-Epilepsy;Nootropics
• Specific: COA
• Test Method: HPLC
• Shelf Life: 2 Years
• CAS No.: 102767-28-2
• Mf: C8h14n2o2
• MW: 170.20896
• Density: 1.168
• Boiling Point: 239.8 °c at 760 Mmhg
• Transport Package: Negotiable
• Specification: 99%
• Trademark: D-sung
• Origin: Shaanxi Xi′an
• Production Capacity: 500kg/Month

Product Description

Pharmaceutical Levetiracetam Sodium Capsule Purity Levetiracetam Powder Material Levetiracetam

Product Description

Product Details

Product name	Levetiracetam
Cas number	102767-28-2
Appearance	White powder
MF	C8H14N2O2
MW	170.20896

Levetiracetam, alias levanteracetam, levitestat, levetiracetam, is a white crystalline powder chemical. Chemical name (S) -α-ethyl-2-oxo-1-pyrrolidine acetamide, molecular formula C8H14N2O2, molecular weight of 170.20900. Levetiracetam as antiepileptic drugs, clinically mainly for adults and children over the age of 4 epilepsy partial seizures plus treatment.

Application&Function

Function of Levetiracetam

Levetiracetam, marketed under the trade names Keppra among others, is a medication used to treat epilepsy. It is used for partial onset, myoclonic, or tonic-clonic seizures. It is the S-enantiomer of etiracetam.
Levetiracetam is available by mouth in two forms: immediate release and extended release.[3] It is also available by injection. An immediate release tablet has been available as a generic in the United States since November 2008, and in the UK since 2011.  The United States patent for the extended release tablet will expire on September 17, 2028. It was initially patented by UCB Pharma. 

Application of Levetiracetam

Levetiracetam has been approved in the United States as add-on treatment for partial (focal), myoclonic, and tonic-clonic seizures. Levetiracetam has been approved in the European Union as a monotherapy treatment for epilepsy in the case of partial seizures, or as an adjunctive therapy for partial, myoclonic, and tonic-clonic seizures. Levetiracetam has been shown to reduce partial (focal) seizures by 50% or more as an add-on medication. It is also used in veterinary medicine for similar purposes.
Levetiracetam is sometimes used off-label to treat status epilepticus or to prevent seizures associated with subarachnoid hemorrhages.
Levetiracetam has potential benefits for other psychiatric and neurologic conditions such as Tourette syndrome,anxiety disorder,[and Alzheimer's disease.However, its most serious adverse effects are behavioral, and its benefit-risk ratio in these conditions is not well understood.
Levetiracetam has not been found to be useful for treatment of neuropathic pain,nor for treatment of essential tremors.Levetiracetam has not been found to be useful for treating autism, but is an effective treatment for partial, myoclonic, or tonic-clonic seizures associated with autism spectrum disorder.

Specification