Neuland Laboratories- A dedicated 100% API provider.
01 1Neuland Laboratories Limited
02 1Cambrex Profarmaco Milano Srl
01 1Aging Life Science Co., Ltd.
02 1Samoh Pharmaceutical Co., Ltd.
01 2Salbutamol sulfate
01 1India
02 1U.S.A
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2021-05-11
Registration Number : 20210511-209-J-985
Manufacturer Name : Neuland Laboratories Limited
Manufacturer Address : Unit 1, Sy. No. 347, 473, 474, 490/2, Bonthapalli Village, Veerabhadraswamy Temple ro...
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2022-08-01
Registration Number : 20220801-209-J-1293
Manufacturer Name : Cambrex Profarmaco Milano Sr...
Manufacturer Address : Via Curiel, 34 – 20067 Paullo (Milan) Italy
A Salbutamol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salbutamol, including repackagers and relabelers. The FDA regulates Salbutamol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salbutamol 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 Salbutamol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Salbutamol supplier is an individual or a company that provides Salbutamol active pharmaceutical ingredient (API) or Salbutamol finished formulations upon request. The Salbutamol suppliers may include Salbutamol API manufacturers, exporters, distributors and traders.
click here to find a list of Salbutamol 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 Salbutamol Drug Master File in Korea (Salbutamol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Salbutamol. The MFDS reviews the Salbutamol KDMF as part of the drug registration process and uses the information provided in the Salbutamol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Salbutamol 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 Salbutamol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Salbutamol suppliers with KDMF on PharmaCompass.
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