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 Ventolin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ventolin, including repackagers and relabelers. The FDA regulates Ventolin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ventolin 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 Ventolin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ventolin supplier is an individual or a company that provides Ventolin active pharmaceutical ingredient (API) or Ventolin finished formulations upon request. The Ventolin suppliers may include Ventolin API manufacturers, exporters, distributors and traders.
click here to find a list of Ventolin 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 Ventolin Drug Master File in Korea (Ventolin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ventolin. The MFDS reviews the Ventolin KDMF as part of the drug registration process and uses the information provided in the Ventolin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ventolin 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 Ventolin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ventolin suppliers with KDMF on PharmaCompass.
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