USP Pharmaceutical Grade Ledipasvir

• Powder: Yes
• Customized: Non-Customized
• Certification: GMP, ISO 9001, USP
• Suitable for: Adult
• State: Solid
• Purity: >99%
• Model NO.: Ledipasvir
• Product Name: Ledipasvir
• Botanical Name: Ledipasvir Powder
• Brand: Zebrago
• Appearance: White Powder
• Test Method: HPLC
• Molecular Formula: C38h72n2o12
• Use: Phamaceutical Intermediates
• Grade: Phamaceutical Grade
• Function: Phamaceutical Intermediates
• CAS No: 1256388-51-8
• Storage: Store in a Cool and Dry Place
• Free Sample: 10 Grams Available
• Apply: Central Antitussive Drug
• Solubility: Soluble in Acetone, Very Slightly Soluble in Hot
• Shipment: by FedEx DHL
• Transport Package: Drum
• Specification: 99% Min
• Trademark: Zebrago
• Origin: China
• HS Code: 2932999099
• Production Capacity: 1000kg/Year

Product Description

Name	Ledipasvir
Synonyms	GS 588
Brand	Zebrago
Molecular Formula	C49H54F2N8O6
Molecular Weight	889.00
CAS NO	1256388-51-8

Ledipasvir is a direct acting antiviral (DAA) medication used as part of combination therapy to treat chronic Hepatitis C, an infectious liver disease caused by infection with Hepatitis C Virus (HCV). After completing Phase III clinical trials, on February 10, 2014 Gilead filed for U.S. approval of a ledipasvir/sofosbuvir fixed-dose combination tablet for genotype 1 hepatitis C.The ledipasvir/sofosbuvir combination is a direct-acting antiviral agent that interferes with HCV replication and can be used to treat patients with genotypes 1a or 1b without PEG-interferon or ribavirin.
Ledipasvir is a potent inhibitor of HCV NS5A, a viral phosphoprotein that plays an important role in viral replication, assembly, and secretion, a hepatitis C virus protein.

 Ledipasvir is an orally available inhibitor of the hepatitis C virus (HCV) non-structural protein 5A (NS5A) replication complex,  ledipasvir is indicated for the treatment of HCV genotypes 1, 4, 5, and 6. Its use has also proven successful in the treatment of HCV in patients co-infected with HIV.

Certificate of Analysis

Batch Number		Z20190412001
Production Date		2019.04.12
Batch Quantity		80 KGS
Item	Test Standard		Testing Result
Appearance	Powder		Complies
Color	White fine Powder		Complies
Particle Size	100% pass 80 mesh		Complies
Oder	Characteristic		Complies
Taste	Characteristic		Complies
Loss on Drying	≤5.0%		2.20%
Residue on Ignition	≤0.1%		0.05%
Residual acetone	≤0.1%		Complies
Residual Ethanol	≤0.5%		Complies
Heave Mentals	≤10ppm		Complies
Na	≤0.1%		<0.1%
Pb	≤3 ppm		Complies
Total Plate	<1000CFU/g		Complies
Yeast & Mold	<100 CFU /g		Complies
E. Coli	Negative		Complies
Salmonella	Negative		Complies
Conclusion: Conform with USP Standard

Storage:Closed container. dry & cool. keep away from moisture &strong light
Shelf life:24 Months  

 

Shipping Options as follows
 

EMS	Around 7-10 working days
DHL	Around 3-5 working days
Fedex	Around 4-6 working days
TNT	Around 6-7 working days
By Air	Around 5-7 working days
By Sea	Around 15-30 working days

     

Perfect After-Sales Service

1. Product Pictures Showing
2. Shipment Tracking Number
3. Promptly Following Tracking Status
4. Delivery Notice
5. Product Quality Following
6. Product Feedback
7. Follow-up Improvement Suggestion

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