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01 1Avik Pharmaceutical Limited
02 1Symbiotica Specialty Ingredients Sdn. Bhd.
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01 1Ace Biopharm Co., Ltd.
02 1Hiple Co., Ltd.
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01 2betamethasone dipropionate
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01 1India
02 1Malaysia
Registrant Name : Hiple Co., Ltd.
Registration Date : 2021-04-27
Registration Number : 20210427-211-J-955
Manufacturer Name : Avik Pharmaceutical Limited
Manufacturer Address : A-1/7 & A-1/8, 1ST Phase, GIDC, City : Vapi - 396 195, Dist. Valsad, Gujarat State, I...
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2021-12-21
Registration Number : 20211221-211-J-1097
Manufacturer Name : Symbiotica Specialty Ingredi...
Manufacturer Address : No. 518, Jalan Waja 4, Taman Industri Waja, 09000 Kulim, Kedah, Malaysia
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PharmaCompass offers a list of Betamethasone Dipropionate 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 Betamethasone Dipropionate manufacturer or Betamethasone Dipropionate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Betamethasone Dipropionate manufacturer or Betamethasone Dipropionate supplier.
PharmaCompass also assists you with knowing the Betamethasone Dipropionate API Price utilized in the formulation of products. Betamethasone Dipropionate API Price is not always fixed or binding as the Betamethasone Dipropionate Price is obtained through a variety of data sources. The Betamethasone Dipropionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SERNIVO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SERNIVO, including repackagers and relabelers. The FDA regulates SERNIVO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SERNIVO 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 SERNIVO manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SERNIVO supplier is an individual or a company that provides SERNIVO active pharmaceutical ingredient (API) or SERNIVO finished formulations upon request. The SERNIVO suppliers may include SERNIVO API manufacturers, exporters, distributors and traders.
click here to find a list of SERNIVO 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 SERNIVO Drug Master File in Korea (SERNIVO KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of SERNIVO. The MFDS reviews the SERNIVO KDMF as part of the drug registration process and uses the information provided in the SERNIVO KDMF to evaluate the safety and efficacy of the drug.
After submitting a SERNIVO 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 SERNIVO API can apply through the Korea Drug Master File (KDMF).
click here to find a list of SERNIVO suppliers with KDMF on PharmaCompass.
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