01 1Johnson & Johnson Innovative Medicine
01 1VOROZOLE DRUG SUBSTANCE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11035
Submission : 1994-08-16
Status : Inactive
Type : II
A Vorozole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vorozole, including repackagers and relabelers. The FDA regulates Vorozole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vorozole 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 Vorozole supplier is an individual or a company that provides Vorozole active pharmaceutical ingredient (API) or Vorozole finished formulations upon request. The Vorozole suppliers may include Vorozole API manufacturers, exporters, distributors and traders.
click here to find a list of Vorozole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vorozole DMF (Drug Master File) is a document detailing the whole manufacturing process of Vorozole active pharmaceutical ingredient (API) in detail. Different forms of Vorozole DMFs exist exist since differing nations have different regulations, such as Vorozole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vorozole DMF submitted to regulatory agencies in the US is known as a USDMF. Vorozole USDMF includes data on Vorozole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vorozole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vorozole suppliers with USDMF on PharmaCompass.
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