Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
01 1M/s Synnat Pharma Pvt ltd
02 1M/s Saurav Chemicals
03 1M/s Saurav Chemicals Ltd
01 1Papaverine HCl IH
02 1Papaverine hydrochloride BP/EP/USP
03 1Papaverine, hydrochloride IH/USP/EP
01 1WC-0171
02 1WC-0171A3
03 1WC-301n
01 3India
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Papaverine hydrochloride BP/EP/USP
Date of Issue : 2021-06-03
Valid Till : 2024-02-07
Written Confirmation Number : WC-301n
Address of the Firm : Plot No 60A, Jawaharlal Nehru Pharma City, Parawada Mandal, Vishakhapatnam, Andh...
Papaverine, hydrochloride IH/USP/EP
Date of Issue : 2022-11-02
Valid Till : 2025-08-13
Written Confirmation Number : WC-0171
Address of the Firm : Deravassi- Barwala Road Village-Bhagwanpura, Teh Bhagwanpura, Derabassi, Dist- S...
Date of Issue : 2021-08-27
Valid Till : 2022-08-13
Written Confirmation Number : WC-0171A3
Address of the Firm : (Unit-III), Village-Bhagwanpur, Barwala Road, Derabassi, Dist-Mohali (Punjab)
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A Paveron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paveron, including repackagers and relabelers. The FDA regulates Paveron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paveron 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 Paveron supplier is an individual or a company that provides Paveron active pharmaceutical ingredient (API) or Paveron finished formulations upon request. The Paveron suppliers may include Paveron API manufacturers, exporters, distributors and traders.
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A Paveron written confirmation (Paveron WC) is an official document issued by a regulatory agency to a Paveron manufacturer, verifying that the manufacturing facility of a Paveron active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Paveron APIs or Paveron finished pharmaceutical products to another nation, regulatory agencies frequently require a Paveron WC (written confirmation) as part of the regulatory process.
click here to find a list of Paveron suppliers with Written Confirmation (WC) on PharmaCompass.
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