01 1SpecGx LLC
01 1Nosa Chemical Co., Ltd.
01 1hydrocodone tartrate
01 1Ireland
Registrant Name : Nosa Chemical Co., Ltd.
Registration Date : 2022-05-25
Registration Number : 20220525-211-J-1305
Manufacturer Name : SpecGx LLC
Manufacturer Address : 3600 North 2nd Street, St. Louis, MO 63147, USA
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PharmaCompass offers a list of Hydrocodone Bitartrate 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 Hydrocodone Bitartrate manufacturer or Hydrocodone Bitartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocodone Bitartrate manufacturer or Hydrocodone Bitartrate supplier.
PharmaCompass also assists you with knowing the Hydrocodone Bitartrate API Price utilized in the formulation of products. Hydrocodone Bitartrate API Price is not always fixed or binding as the Hydrocodone Bitartrate Price is obtained through a variety of data sources. The Hydrocodone Bitartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ANEXSIA 5/325-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ANEXSIA 5/325-1, including repackagers and relabelers. The FDA regulates ANEXSIA 5/325-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ANEXSIA 5/325-1 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 ANEXSIA 5/325-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ANEXSIA 5/325-1 supplier is an individual or a company that provides ANEXSIA 5/325-1 active pharmaceutical ingredient (API) or ANEXSIA 5/325-1 finished formulations upon request. The ANEXSIA 5/325-1 suppliers may include ANEXSIA 5/325-1 API manufacturers, exporters, distributors and traders.
click here to find a list of ANEXSIA 5/325-1 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 ANEXSIA 5/325-1 Drug Master File in Korea (ANEXSIA 5/325-1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of ANEXSIA 5/325-1. The MFDS reviews the ANEXSIA 5/325-1 KDMF as part of the drug registration process and uses the information provided in the ANEXSIA 5/325-1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a ANEXSIA 5/325-1 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 ANEXSIA 5/325-1 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of ANEXSIA 5/325-1 suppliers with KDMF on PharmaCompass.
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