01 1FDC
01 1CINNARIZINE
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31934
Submission : 2017-09-07
Status : Active
Type : II
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A Stugeron Forte manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stugeron Forte, including repackagers and relabelers. The FDA regulates Stugeron Forte manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stugeron Forte 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 Stugeron Forte manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Stugeron Forte supplier is an individual or a company that provides Stugeron Forte active pharmaceutical ingredient (API) or Stugeron Forte finished formulations upon request. The Stugeron Forte suppliers may include Stugeron Forte API manufacturers, exporters, distributors and traders.
click here to find a list of Stugeron Forte suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Stugeron Forte DMF (Drug Master File) is a document detailing the whole manufacturing process of Stugeron Forte active pharmaceutical ingredient (API) in detail. Different forms of Stugeron Forte DMFs exist exist since differing nations have different regulations, such as Stugeron Forte USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Stugeron Forte DMF submitted to regulatory agencies in the US is known as a USDMF. Stugeron Forte USDMF includes data on Stugeron Forte's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Stugeron Forte USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Stugeron Forte suppliers with USDMF on PharmaCompass.
