01 1Priti Industries
01 1ALMAGATE EP/BP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38894
Submission : 2023-11-18
Status : Active
Type : II
A Almagate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Almagate, including repackagers and relabelers. The FDA regulates Almagate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Almagate 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 Almagate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Almagate supplier is an individual or a company that provides Almagate active pharmaceutical ingredient (API) or Almagate finished formulations upon request. The Almagate suppliers may include Almagate API manufacturers, exporters, distributors and traders.
click here to find a list of Almagate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Almagate DMF (Drug Master File) is a document detailing the whole manufacturing process of Almagate active pharmaceutical ingredient (API) in detail. Different forms of Almagate DMFs exist exist since differing nations have different regulations, such as Almagate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Almagate DMF submitted to regulatory agencies in the US is known as a USDMF. Almagate USDMF includes data on Almagate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Almagate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Almagate suppliers with USDMF on PharmaCompass.
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