Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Laboratorium Ofichem B.V
02 1Jubilant Generics
01 1HISTAMINE DI-HYDROCHLORIDE
02 1HISTAMINE DIHYDROCHLORIDE
01 1India
02 1Netherlands
01 2Active
01 2Blank
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34358
Submission : 2020-03-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35554
Submission : 2021-03-31
Status : Active
Type : II
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard, including repackagers and relabelers. The FDA regulates Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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 Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard supplier is an individual or a company that provides Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard active pharmaceutical ingredient (API) or Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard finished formulations upon request. The Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers may include Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard DMF (Drug Master File) is a document detailing the whole manufacturing process of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard active pharmaceutical ingredient (API) in detail. Different forms of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard DMFs exist exist since differing nations have different regulations, such as Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard DMF submitted to regulatory agencies in the US is known as a USDMF. Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard USDMF includes data on Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers with USDMF on PharmaCompass.
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