Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
01 1M/s. Synnat Pharma Private Limited
02 2M/s SCL Lifesciences Limited
01 1Papaverine Hydrochloride BP/USP/Ph. Eur.
02 1Papaverine Hydrochloride IH
03 1Papaverine Hydrochloride USP/Ph. Eur
01 2WC-0171
02 1WC-0301
01 3India
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Papaverine Hydrochloride BP/USP/Ph. Eur.
Date of Issue : 2024-05-22
Valid Till : 2027-07-02
Written Confirmation Number : WC-0301
Address of the Firm : Plot No. 60A, Jawaharlal Nehru Pharma City, Parawada Mandal, Anakapalli District...
Date of Issue : 2022-11-02
Valid Till : 2025-08-13
Written Confirmation Number : WC-0171
Address of the Firm : Village Bhagwanpura, Derabassi - Barwala Road, Tehsil: Derabassi, District: Sahi...
Papaverine Hydrochloride USP/Ph. Eur
Date of Issue : 2022-11-02
Valid Till : 2025-08-13
Written Confirmation Number : WC-0171
Address of the Firm : Village Bhagwanpura, Derabassi - Barwala Road, Tehsil: Derabassi, District: Sahi...
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PharmaCompass offers a list of Papaverine Hydrochloride 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 Papaverine Hydrochloride manufacturer or Papaverine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Papaverine Hydrochloride API Price utilized in the formulation of products. Papaverine Hydrochloride API Price is not always fixed or binding as the Papaverine Hydrochloride Price is obtained through a variety of data sources. The Papaverine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vaso-Pav manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vaso-Pav, including repackagers and relabelers. The FDA regulates Vaso-Pav manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vaso-Pav API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Vaso-Pav supplier is an individual or a company that provides Vaso-Pav active pharmaceutical ingredient (API) or Vaso-Pav finished formulations upon request. The Vaso-Pav suppliers may include Vaso-Pav API manufacturers, exporters, distributors and traders.
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A Vaso-Pav written confirmation (Vaso-Pav WC) is an official document issued by a regulatory agency to a Vaso-Pav manufacturer, verifying that the manufacturing facility of a Vaso-Pav active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vaso-Pav APIs or Vaso-Pav finished pharmaceutical products to another nation, regulatory agencies frequently require a Vaso-Pav WC (written confirmation) as part of the regulatory process.
click here to find a list of Vaso-Pav suppliers with Written Confirmation (WC) on PharmaCompass.
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