Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
01 1Synnat Pharma Private Limited
02 1SCL Lifesciences Limited
01 1Daeshin Pharmaceutical Co., Ltd.
02 1Hiple Co., Ltd.
01 2papaverine hydrochloride
01 2India
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2025-05-09
Registration Number : 20250509-211-J-1860
Manufacturer Name : Synnat Pharma Private Limite...
Manufacturer Address : Plot No.60A, Jawaharlal Nehru Pharma City, Parawada Mandal, Vishakhapatnam-531019. An...
Registrant Name : Hiple Co., Ltd.
Registration Date : 2025-03-24
Registration Number : 20250324-211-J-1789
Manufacturer Name : SCL Lifesciences Limited
Manufacturer Address : Derabassi–Barwala Road, Village Bhagwanpura, Tehsil Derabassi, District Sahibzada A...
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Papaverine Hydrochloride manufacturer or Papaverine Hydrochloride supplier.
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.
click here to find a list of Vaso-Pav manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
click here to find a list of Vaso-Pav suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Vaso-Pav Drug Master File in Korea (Vaso-Pav KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Vaso-Pav. The MFDS reviews the Vaso-Pav KDMF as part of the drug registration process and uses the information provided in the Vaso-Pav KDMF to evaluate the safety and efficacy of the drug.
After submitting a Vaso-Pav KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Vaso-Pav API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Vaso-Pav suppliers with KDMF on PharmaCompass.
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