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01 1S D Fine Chem Limited
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01 1SODIUM HYDROXIDE PELLETS BP
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01 1India
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01 1Active
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28719
Submission : 2014-10-03
Status : Active
Type : IV
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PharmaCompass offers a list of Sodium Hydroxide 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 Sodium Hydroxide manufacturer or Sodium Hydroxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Hydroxide manufacturer or Sodium Hydroxide supplier.
PharmaCompass also assists you with knowing the Sodium Hydroxide API Price utilized in the formulation of products. Sodium Hydroxide API Price is not always fixed or binding as the Sodium Hydroxide Price is obtained through a variety of data sources. The Sodium Hydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C12569 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C12569, including repackagers and relabelers. The FDA regulates C12569 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C12569 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 C12569 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C12569 supplier is an individual or a company that provides C12569 active pharmaceutical ingredient (API) or C12569 finished formulations upon request. The C12569 suppliers may include C12569 API manufacturers, exporters, distributors and traders.
click here to find a list of C12569 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C12569 DMF (Drug Master File) is a document detailing the whole manufacturing process of C12569 active pharmaceutical ingredient (API) in detail. Different forms of C12569 DMFs exist exist since differing nations have different regulations, such as C12569 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A C12569 DMF submitted to regulatory agencies in the US is known as a USDMF. C12569 USDMF includes data on C12569's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The C12569 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of C12569 suppliers with USDMF on PharmaCompass.
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