01 1Dynamit Nobel GmbH
01 1Encomac Co., Ltd.
01 1nitroglycerin
01 1Germany
Registrant Name : Encomac Co., Ltd.
Registration Date : 2021-11-10
Registration Number : 20211110-210-J-1146
Manufacturer Name : Dynamit Nobel GmbH
Manufacturer Address : D-51377, Kalkstrasse 218 Leverkusen, Germany
38
PharmaCompass offers a list of Nitroglycerin 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 Nitroglycerin manufacturer or Nitroglycerin supplier for your needs.
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A Nitro Mack Retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nitro Mack Retard, including repackagers and relabelers. The FDA regulates Nitro Mack Retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nitro Mack Retard 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 Nitro Mack Retard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Nitro Mack Retard supplier is an individual or a company that provides Nitro Mack Retard active pharmaceutical ingredient (API) or Nitro Mack Retard finished formulations upon request. The Nitro Mack Retard suppliers may include Nitro Mack Retard API manufacturers, exporters, distributors and traders.
click here to find a list of Nitro Mack Retard 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 Nitro Mack Retard Drug Master File in Korea (Nitro Mack Retard KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nitro Mack Retard. The MFDS reviews the Nitro Mack Retard KDMF as part of the drug registration process and uses the information provided in the Nitro Mack Retard KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nitro Mack Retard 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 Nitro Mack Retard API can apply through the Korea Drug Master File (KDMF).
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