01 1Siegfried AG
01 1AMOBARBITAL SODIUM USP
01 1Switzerland
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1051
Submission : 1967-03-23
Status : Active
Type : II
85
PharmaCompass offers a list of Amobarbital Sodium 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 Amobarbital Sodium manufacturer or Amobarbital Sodium supplier for your needs.
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A Dorminal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dorminal, including repackagers and relabelers. The FDA regulates Dorminal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dorminal API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Dorminal supplier is an individual or a company that provides Dorminal active pharmaceutical ingredient (API) or Dorminal finished formulations upon request. The Dorminal suppliers may include Dorminal API manufacturers, exporters, distributors and traders.
click here to find a list of Dorminal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dorminal DMF (Drug Master File) is a document detailing the whole manufacturing process of Dorminal active pharmaceutical ingredient (API) in detail. Different forms of Dorminal DMFs exist exist since differing nations have different regulations, such as Dorminal USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dorminal DMF submitted to regulatory agencies in the US is known as a USDMF. Dorminal USDMF includes data on Dorminal's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dorminal USDMF is kept confidential to protect the manufacturer’s intellectual property.
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