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