Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Alivus Life Sciences
03 1Honour Lab
04 1MSN Laboratories
05 1Taro Pharmaceutical Industries
01 5TAVABOROLE
01 4India
02 1U.S.A
01 5Active
01 5Complete
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Complete
Rev. Date : 2017-04-17
Pay. Date : 2017-03-13
DMF Number : 31431
Submission : 2017-03-02
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-03-23
Pay. Date : 2017-03-09
DMF Number : 31283
Submission : 2017-01-31
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-05-24
Pay. Date : 2018-03-05
DMF Number : 32533
Submission : 2018-04-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-05-09
Pay. Date : 2018-03-14
DMF Number : 32154
Submission : 2017-10-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-06-06
Pay. Date : 2018-03-27
DMF Number : 32083
Submission : 2018-03-26
Status : Active
Type : II
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PharmaCompass offers a list of Tavaborole 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 Tavaborole manufacturer or Tavaborole supplier for your needs.
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PharmaCompass also assists you with knowing the Tavaborole API Price utilized in the formulation of products. Tavaborole API Price is not always fixed or binding as the Tavaborole Price is obtained through a variety of data sources. The Tavaborole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KERYDIN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KERYDIN, including repackagers and relabelers. The FDA regulates KERYDIN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KERYDIN 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 KERYDIN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KERYDIN supplier is an individual or a company that provides KERYDIN active pharmaceutical ingredient (API) or KERYDIN finished formulations upon request. The KERYDIN suppliers may include KERYDIN API manufacturers, exporters, distributors and traders.
click here to find a list of KERYDIN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KERYDIN DMF (Drug Master File) is a document detailing the whole manufacturing process of KERYDIN active pharmaceutical ingredient (API) in detail. Different forms of KERYDIN DMFs exist exist since differing nations have different regulations, such as KERYDIN USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A KERYDIN DMF submitted to regulatory agencies in the US is known as a USDMF. KERYDIN USDMF includes data on KERYDIN's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The KERYDIN USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of KERYDIN suppliers with USDMF on PharmaCompass.
We have 5 companies offering KERYDIN
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