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01 1Purisys LLC
02 1FineTech Pharmaceutical Ltd.
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01 1NABILONE
02 1NABILONE DRUG SUBSTANCE
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01 1Israel
02 1U.S.A
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01 2Active
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01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35408
Submission : 2020-12-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31946
Submission : 2017-08-14
Status : Active
Type : II
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PharmaCompass offers a list of Nabilone 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 Nabilone manufacturer or Nabilone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nabilone manufacturer or Nabilone supplier.
PharmaCompass also assists you with knowing the Nabilone API Price utilized in the formulation of products. Nabilone API Price is not always fixed or binding as the Nabilone Price is obtained through a variety of data sources. The Nabilone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 51022-71-0 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 51022-71-0, including repackagers and relabelers. The FDA regulates 51022-71-0 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 51022-71-0 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 51022-71-0 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 51022-71-0 supplier is an individual or a company that provides 51022-71-0 active pharmaceutical ingredient (API) or 51022-71-0 finished formulations upon request. The 51022-71-0 suppliers may include 51022-71-0 API manufacturers, exporters, distributors and traders.
click here to find a list of 51022-71-0 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 51022-71-0 DMF (Drug Master File) is a document detailing the whole manufacturing process of 51022-71-0 active pharmaceutical ingredient (API) in detail. Different forms of 51022-71-0 DMFs exist exist since differing nations have different regulations, such as 51022-71-0 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 51022-71-0 DMF submitted to regulatory agencies in the US is known as a USDMF. 51022-71-0 USDMF includes data on 51022-71-0's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 51022-71-0 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 51022-71-0 suppliers with USDMF on PharmaCompass.
We have 2 companies offering 51022-71-0
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