Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.

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01 1Vamsi Labs
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01 1FENOTEROL HYDROBROMIDE-EP
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01 1India
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Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40580
Submission : 2024-09-26
Status : Active
Type : II
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PharmaCompass offers a list of Fenoterol Hydrobromide 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 Fenoterol Hydrobromide manufacturer or Fenoterol Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Fenoterol Hydrobromide API Price utilized in the formulation of products. Fenoterol Hydrobromide API Price is not always fixed or binding as the Fenoterol Hydrobromide Price is obtained through a variety of data sources. The Fenoterol Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Partusisten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Partusisten, including repackagers and relabelers. The FDA regulates Partusisten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Partusisten 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 Partusisten supplier is an individual or a company that provides Partusisten active pharmaceutical ingredient (API) or Partusisten finished formulations upon request. The Partusisten suppliers may include Partusisten API manufacturers, exporters, distributors and traders.
click here to find a list of Partusisten suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Partusisten DMF (Drug Master File) is a document detailing the whole manufacturing process of Partusisten active pharmaceutical ingredient (API) in detail. Different forms of Partusisten DMFs exist exist since differing nations have different regulations, such as Partusisten USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Partusisten DMF submitted to regulatory agencies in the US is known as a USDMF. Partusisten USDMF includes data on Partusisten's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Partusisten USDMF is kept confidential to protect the manufacturer’s intellectual property.
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