Neuland Laboratories- A dedicated 100% API provider.
01 4Neuland Laboratories Ltd.
02 1Boehringer Ingelheim Pharma GmbH & Co. K.G.
03 1Lusochimica SpA
04 1OLON SPA
05 2Sifavitor Srl
Neuland Laboratories- A dedicated 100% API provider.
Registrant Name : Geonil Pharmaceutical Co., Ltd.
Registration Date : 2013-07-18
Registration Number : 20130614-188-I-356-02(2)
Manufacturer Name : Neuland Laboratories Ltd.
Manufacturer Address : Unit-I, Sy. No: 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy Temple Ro...
Neuland Laboratories- A dedicated 100% API provider.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-07-02
Registration Number : 20130614-188-I-356-02(A)
Manufacturer Name : Neuland Laboratories Ltd.
Manufacturer Address : Unit-I, Sy. No: 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy Temple Ro...
Neuland Laboratories- A dedicated 100% API provider.
Registrant Name : Hanlim Pharmaceutical Co., Ltd.
Registration Date : 2013-07-18
Registration Number : 20130614-188-I-356-02(1)
Manufacturer Name : Neuland Laboratories Ltd.
Manufacturer Address : Unit I, Sy. No: 347,473, 474, 490/2 Bonthapally Village Veerabhadraswamy Temple Road,...
Neuland Laboratories- A dedicated 100% API provider.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2013-06-14
Registration Number : 20130614-188-I-356-02
Manufacturer Name : Neuland Laboratories Ltd.
Manufacturer Address : Unit-I, Sy. No: 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy Temple Ro...
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PharmaCompass offers a list of Ipratropium Bromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ipratropium Bromide manufacturer or Ipratropium Bromide supplier for your needs.
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A COMBIVENT-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of COMBIVENT-1, including repackagers and relabelers. The FDA regulates COMBIVENT-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. COMBIVENT-1 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A COMBIVENT-1 supplier is an individual or a company that provides COMBIVENT-1 active pharmaceutical ingredient (API) or COMBIVENT-1 finished formulations upon request. The COMBIVENT-1 suppliers may include COMBIVENT-1 API manufacturers, exporters, distributors and traders.
click here to find a list of COMBIVENT-1 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 COMBIVENT-1 Drug Master File in Korea (COMBIVENT-1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of COMBIVENT-1. The MFDS reviews the COMBIVENT-1 KDMF as part of the drug registration process and uses the information provided in the COMBIVENT-1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a COMBIVENT-1 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 COMBIVENT-1 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of COMBIVENT-1 suppliers with KDMF on PharmaCompass.
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