Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Ofichem BV
02 1Jubilant Pharmova Limited
01 1Histamine Dihydrochloride
02 1histamine dihydrochloride
01 1India
02 1Netherlands
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-0969
Start Marketing Date : 2017-12-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1207
Start Marketing Date : 2021-09-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Histamine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histamine Dihydrochloride, including repackagers and relabelers. The FDA regulates Histamine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histamine Dihydrochloride 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histamine Dihydrochloride supplier is an individual or a company that provides Histamine Dihydrochloride active pharmaceutical ingredient (API) or Histamine Dihydrochloride finished formulations upon request. The Histamine Dihydrochloride suppliers may include Histamine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Histamine Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Histamine Dihydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Histamine Dihydrochloride API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Histamine Dihydrochloride as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Histamine Dihydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Histamine Dihydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Histamine Dihydrochloride suppliers with NDC on PharmaCompass.
We have 2 companies offering Histamine Dihydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
