01 1BASF SE
02 1Zhejiang NHU Company Ltd.
01 1Narsha Farm Co., Ltd.
02 1Pharmaline Co., Ltd.
01 2Tocopherol acetate
01 1China
02 1Germany
Registrant Name : Pharmaline Co., Ltd.
Registration Date : 2024-08-09
Registration Number : 20240809-211-J-1635
Manufacturer Name : BASF SE
Manufacturer Address : Carl-Bosch-Strasse 38, 67056 Ludwigshafen, Germany
Registrant Name : Narsha Farm Co., Ltd.
Registration Date : 2025-06-17
Registration Number : 20250617-211-J-1918
Manufacturer Name : Zhejiang NHU Company Ltd.
Manufacturer Address : No. 428 Xinchang Dadao West Road, Qixing Street, Xinchang County, Zhejiang Province, ...
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PharmaCompass offers a list of Vitamin E Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Vitamin E Acetate manufacturer or Vitamin E Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin E Acetate manufacturer or Vitamin E Acetate supplier.
A INFUVITE ADULT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INFUVITE ADULT, including repackagers and relabelers. The FDA regulates INFUVITE ADULT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INFUVITE ADULT 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 INFUVITE ADULT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A INFUVITE ADULT supplier is an individual or a company that provides INFUVITE ADULT active pharmaceutical ingredient (API) or INFUVITE ADULT finished formulations upon request. The INFUVITE ADULT suppliers may include INFUVITE ADULT API manufacturers, exporters, distributors and traders.
click here to find a list of INFUVITE ADULT suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 INFUVITE ADULT Drug Master File in Korea (INFUVITE ADULT KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of INFUVITE ADULT. The MFDS reviews the INFUVITE ADULT KDMF as part of the drug registration process and uses the information provided in the INFUVITE ADULT KDMF to evaluate the safety and efficacy of the drug.
After submitting a INFUVITE ADULT 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 INFUVITE ADULT API can apply through the Korea Drug Master File (KDMF).
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