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| Molecular Weight | 324.34 g/mol |
|---|---|
| Molecular Formula | C13H20N6O4 |
| XLogP3 | -0.5 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 8 |
| Exact Mass | 324.15460314 g/mol |
| Monoisotopic Mass | 324.15460314 g/mol |
| Topological Polar Surface Area | 147 A^2 |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 483 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
| 1 of 2 | |
|---|---|
| Drug Name | Valtrex |
| PubMed Health | Valacyclovir (By mouth) |
| Drug Classes | Antiviral |
| Drug Label | VALTREX (valacyclovir hydrochloride) is the hydrochloride salt of the L-valyl ester of the antiviral drug acyclovir.VALTREX Caplets are for oral administration. Each caplet contains valacyclovir hydrochloride equivalent to 500mg or 1gram valacycl... |
| Active Ingredient | Valacyclovir hydrochloride |
| Dosage Form | Tablet |
| Route | oral; Oral |
| Strength | eq 500mg base; eq 1gm base |
| Market Status | Prescription |
| Company | Glaxosmithkline |
| 2 of 2 | |
|---|---|
| Drug Name | Valtrex |
| PubMed Health | Valacyclovir (By mouth) |
| Drug Classes | Antiviral |
| Drug Label | VALTREX (valacyclovir hydrochloride) is the hydrochloride salt of the L-valyl ester of the antiviral drug acyclovir.VALTREX Caplets are for oral administration. Each caplet contains valacyclovir hydrochloride equivalent to 500mg or 1gram valacycl... |
| Active Ingredient | Valacyclovir hydrochloride |
| Dosage Form | Tablet |
| Route | oral; Oral |
| Strength | eq 500mg base; eq 1gm base |
| Market Status | Prescription |
| Company | Glaxosmithkline |
API SUPPLIERS
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Together we can improve the quality of life
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm :
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EU WC
Valaciclovir Hydrochloride Hydrated Ph.Eur
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm : Plot No. 35, 36, 38, 39, 40, 49, 50 & 51, Phase-IV, IDA, Jeedimetla, Medchal-Mal...
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
Together we can improve the quality of life
About the Company : Shamrock Pharmachemi Pvt Ltd. is a globally recognized API leader with over 26 years of expertise in human and veterinary pharmaceuticals. Operating in 40+ countries, we own two st...
About the Company : Amara Labs Pvt Ltd is a WHO-GMP certified manufacturing company wholly owned by a team of technocrats with working experience of more than 20 years in Multi-Nationals Companies lik...
About the Company : Founded in 1986 by Mr. P.V. Ramaprasad Reddy, Mr. K. Nityananda Reddy and a small group of highly committed professionals, Aurobindo Pharma was born off a vision. The company comme...
About the Company : Exemed, with due global accreditations from US FDA, KFDA and other regulatory bodies, is one of the leading and cost-competitive manufacturers of Metformin. Besides Metformin we ma...
About the Company : Harman Finochem Limited is a leading India-based Pharmaceutical Company which specializes in the manufacture and export of more than 45 Active Pharmaceutical Ingredients (APls) of ...
About the Company : JIN DUN Medical Research Institute is affiliated to Shanghai JIN DUN Industrial Co., Ltd., headquartered in Shanghai, adjacent to Hongqiao High-speed Railway Station and Hongqiao I...
About the Company : Piramal Pharma Solutions (PPS) is a CDMO that provides end-to-end solutions for drug development and manufacturing across the drug life cycle to its clients in North America, Europ...
About the Company : The technology of production of artemisinin and its derivatives is based on the use of cultivation of annual wormwood cells and extraction of artemisinin and artemisinic acid. Qual...
About the Company : Vital Group of companies is a leading Manufacturer and Exporter of Active Pharmaceutical Ingredients (API). Founded in 1999 Vital set up a unit for manufacturing for Quinine Salts ...
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Average Price (USD/KGS) |
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PharmaCompass offers a list of Valacyclovir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Valacyclovir manufacturer or Valacyclovir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Valacyclovir manufacturer or Valacyclovir supplier.
PharmaCompass also assists you with knowing the Valacyclovir API Price utilized in the formulation of products. Valacyclovir API Price is not always fixed or binding as the Valacyclovir Price is obtained through a variety of data sources. The Valacyclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zelitrex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zelitrex, including repackagers and relabelers. The FDA regulates Zelitrex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zelitrex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Zelitrex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zelitrex supplier is an individual or a company that provides Zelitrex active pharmaceutical ingredient (API) or Zelitrex finished formulations upon request. The Zelitrex suppliers may include Zelitrex API manufacturers, exporters, distributors and traders.
click here to find a list of Zelitrex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zelitrex written confirmation (Zelitrex WC) is an official document issued by a regulatory agency to a Zelitrex manufacturer, verifying that the manufacturing facility of a Zelitrex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zelitrex APIs or Zelitrex finished pharmaceutical products to another nation, regulatory agencies frequently require a Zelitrex WC (written confirmation) as part of the regulatory process.
click here to find a list of Zelitrex suppliers with Written Confirmation (WC) on PharmaCompass.
Zelitrex Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Zelitrex GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Zelitrex GMP manufacturer or Zelitrex GMP API supplier for your needs.
A Zelitrex CoA (Certificate of Analysis) is a formal document that attests to Zelitrex's compliance with Zelitrex specifications and serves as a tool for batch-level quality control.
Zelitrex CoA mostly includes findings from lab analyses of a specific batch. For each Zelitrex CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Zelitrex may be tested according to a variety of international standards, such as European Pharmacopoeia (Zelitrex EP), Zelitrex JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zelitrex USP).
