01 1Silverline Chemical
01 1THYMOL USP/BP/EP/IP/JP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34458
Submission : 2020-02-17
Status : Active
Type : IV
A Thymol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thymol, including repackagers and relabelers. The FDA regulates Thymol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thymol 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 Thymol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Thymol supplier is an individual or a company that provides Thymol active pharmaceutical ingredient (API) or Thymol finished formulations upon request. The Thymol suppliers may include Thymol API manufacturers, exporters, distributors and traders.
click here to find a list of Thymol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Thymol DMF (Drug Master File) is a document detailing the whole manufacturing process of Thymol active pharmaceutical ingredient (API) in detail. Different forms of Thymol DMFs exist exist since differing nations have different regulations, such as Thymol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Thymol DMF submitted to regulatory agencies in the US is known as a USDMF. Thymol USDMF includes data on Thymol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Thymol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Thymol suppliers with USDMF on PharmaCompass.
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