Inke S.A: APIs manufacturing plant.
01 1INKE SA
02 1Novartis Pharma Schweizerhalle AG@Novartis Pharma AG@Novartis Pharma Stein AG@Sterling Pharma Ringaskiddy Limited@Novartis Pharmaceutical Manufacturing LLC
03 1Novartis Pharma Stein AG@Novartis Pharma AG@Novartis Pharma Schweizerhalle AG@Sterling Pharma Ringaskiddy Limited@Novartis Pharmaceutical Manufacturing LLC
01 2Novartis Korea Ltd.
02 1Samoh Pharmaceutical Co., Ltd.
01 3Indacaterol maleate
01 1Spain
02 2Switzerland
Inke S.A: APIs manufacturing plant.
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2020-10-27
Registration Number : Su207-45-ND
Manufacturer Name : INKE SA
Manufacturer Address : 08755 Area Industrial del Llobregat, C/Argent 1, Castellbisbal Barcelona, Spain
Registrant Name : Novartis Korea Ltd.
Registration Date : 2024-01-29
Registration Number : 196-27-ND
Manufacturer Name : Novartis Pharma Schweizerhal...
Manufacturer Address : Rothausstrasse, 4133, Pratteln, Switzerland@Lichstrasse 35 4056 Basel, Switzerland @S...
Registrant Name : Novartis Korea Ltd.
Registration Date : 2010-05-27
Registration Number : Su163-10-ND
Manufacturer Name : Novartis Pharma Stein AG@Nov...
Manufacturer Address : Schaffhauserstrasse, 4332 Stein, Switzerland@Lichstrasse 35 4056 Basel, Switzerland @...
A Arcapta neohaler (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arcapta neohaler (TN), including repackagers and relabelers. The FDA regulates Arcapta neohaler (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arcapta neohaler (TN) 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 Arcapta neohaler (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arcapta neohaler (TN) supplier is an individual or a company that provides Arcapta neohaler (TN) active pharmaceutical ingredient (API) or Arcapta neohaler (TN) finished formulations upon request. The Arcapta neohaler (TN) suppliers may include Arcapta neohaler (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Arcapta neohaler (TN) 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 Arcapta neohaler (TN) Drug Master File in Korea (Arcapta neohaler (TN) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Arcapta neohaler (TN). The MFDS reviews the Arcapta neohaler (TN) KDMF as part of the drug registration process and uses the information provided in the Arcapta neohaler (TN) KDMF to evaluate the safety and efficacy of the drug.
After submitting a Arcapta neohaler (TN) 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 Arcapta neohaler (TN) API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Arcapta neohaler (TN) suppliers with KDMF on PharmaCompass.
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