01 1Changzhou SynTheAll Pharmaceutical Co., Ltd
02 1Jilin Asymchem Laboratories Co., Ltd
03 1Pfizer Ireland Pharmaceuticals
01 3Korea Pfizer Pharmaceutical Co., Ltd.
01 3Nirmatrelvir
01 1Japan
02 2U.S.A
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2023-07-14
Registration Number : Number 87-33-ND
Manufacturer Name : Changzhou SynTheAll Pharmace...
Manufacturer Address : No. 589 North Yulong Road, Xinbei District Changzhou, CH213127, China
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2023-07-14
Registration Number : Number 87-35-ND
Manufacturer Name : Pfizer Ireland Pharmaceutica...
Manufacturer Address : Ringaskiddy Active Pharmaceutical Ingredient Plant, PO Box 140, Ringaskiddy, County C...
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2023-07-14
Registration Number : Number 87-34-ND
Manufacturer Name : Jilin Asymchem Laboratories ...
Manufacturer Address : No.99, Hongda Road, Economic Development Zone, Dunhua, Jilin, 133700, China
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PharmaCompass offers a list of Nirmatrelvir 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 Nirmatrelvir manufacturer or Nirmatrelvir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nirmatrelvir manufacturer or Nirmatrelvir supplier.
PharmaCompass also assists you with knowing the Nirmatrelvir API Price utilized in the formulation of products. Nirmatrelvir API Price is not always fixed or binding as the Nirmatrelvir Price is obtained through a variety of data sources. The Nirmatrelvir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PF07321332 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PF07321332, including repackagers and relabelers. The FDA regulates PF07321332 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PF07321332 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 PF07321332 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PF07321332 supplier is an individual or a company that provides PF07321332 active pharmaceutical ingredient (API) or PF07321332 finished formulations upon request. The PF07321332 suppliers may include PF07321332 API manufacturers, exporters, distributors and traders.
click here to find a list of PF07321332 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 PF07321332 Drug Master File in Korea (PF07321332 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of PF07321332. The MFDS reviews the PF07321332 KDMF as part of the drug registration process and uses the information provided in the PF07321332 KDMF to evaluate the safety and efficacy of the drug.
After submitting a PF07321332 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 PF07321332 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of PF07321332 suppliers with KDMF on PharmaCompass.
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