Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
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01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Bachem AG
03 1MSN Laboratories
04 1Sun Pharmaceutical Industries Limited
05 1Viatris
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01 4SINCALIDE
02 1Sincalide
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01 3India
02 1Switzerland
03 1U.S.A
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01 5Active
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01 2Complete
02 3Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34202
Submission : 2019-12-17
Status : Active
Type : II
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15165
Submission : 2000-11-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2023-01-09
Pay. Date : 2022-10-25
DMF Number : 36429
Submission : 2021-10-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2025-02-10
Pay. Date : 2025-01-13
DMF Number : 40875
Submission : 2025-01-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32302
Submission : 2018-01-07
Status : Active
Type : II
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PharmaCompass offers a list of Sincalide 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 Sincalide manufacturer or Sincalide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sincalide manufacturer or Sincalide supplier.
PharmaCompass also assists you with knowing the Sincalide API Price utilized in the formulation of products. Sincalide API Price is not always fixed or binding as the Sincalide Price is obtained through a variety of data sources. The Sincalide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Kinevac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kinevac, including repackagers and relabelers. The FDA regulates Kinevac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kinevac 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 Kinevac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Kinevac supplier is an individual or a company that provides Kinevac active pharmaceutical ingredient (API) or Kinevac finished formulations upon request. The Kinevac suppliers may include Kinevac API manufacturers, exporters, distributors and traders.
click here to find a list of Kinevac suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Kinevac DMF (Drug Master File) is a document detailing the whole manufacturing process of Kinevac active pharmaceutical ingredient (API) in detail. Different forms of Kinevac DMFs exist exist since differing nations have different regulations, such as Kinevac USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Kinevac DMF submitted to regulatory agencies in the US is known as a USDMF. Kinevac USDMF includes data on Kinevac's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Kinevac USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Kinevac suppliers with USDMF on PharmaCompass.
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