01 1BASF
02 1Cipla
03 1Divis Laboratories
04 1Olon S.p.A
05 1SREENIVASA PHARMA PRIVATE LTD
06 1Viatris
01 1BTS 54 524
02 1SIBUTRAMINE HYDROCHLORIDE
03 1SIBUTRAMINE HYDROCHLORIDE ANHYDROUS
04 3SIBUTRAMINE HYDROCHLORIDE MONOHYDRATE
01 1Germany
02 3India
03 1Italy
04 1U.S.A
01 6Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6063
Submission : 1985-09-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20161
Submission : 2007-01-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19729
Submission : 2006-09-04
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17171
Submission : 2004-02-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22373
Submission : 2009-01-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17977
Submission : 2005-01-06
Status : Inactive
Type : II
21
PharmaCompass offers a list of Sibutramine Hydrochloride 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 Sibutramine Hydrochloride manufacturer or Sibutramine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sibutramine Hydrochloride manufacturer or Sibutramine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Sibutramine Hydrochloride API Price utilized in the formulation of products. Sibutramine Hydrochloride API Price is not always fixed or binding as the Sibutramine Hydrochloride Price is obtained through a variety of data sources. The Sibutramine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Reductil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Reductil, including repackagers and relabelers. The FDA regulates Reductil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Reductil 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 Reductil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Reductil supplier is an individual or a company that provides Reductil active pharmaceutical ingredient (API) or Reductil finished formulations upon request. The Reductil suppliers may include Reductil API manufacturers, exporters, distributors and traders.
click here to find a list of Reductil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Reductil DMF (Drug Master File) is a document detailing the whole manufacturing process of Reductil active pharmaceutical ingredient (API) in detail. Different forms of Reductil DMFs exist exist since differing nations have different regulations, such as Reductil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Reductil DMF submitted to regulatory agencies in the US is known as a USDMF. Reductil USDMF includes data on Reductil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Reductil USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Reductil suppliers with USDMF on PharmaCompass.
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