01 1Curia
01 131/AC HCL
01 1U.S.A
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12990
Submission : 1998-05-05
Status : Active
Type : II
23
PharmaCompass offers a list of Hydrochloric Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Hydrochloric Acid manufacturer or Hydrochloric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrochloric Acid manufacturer or Hydrochloric Acid supplier.
PharmaCompass also assists you with knowing the Hydrochloric Acid API Price utilized in the formulation of products. Hydrochloric Acid API Price is not always fixed or binding as the Hydrochloric Acid Price is obtained through a variety of data sources. The Hydrochloric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E507 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E507, including repackagers and relabelers. The FDA regulates E507 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E507 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 E507 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E507 supplier is an individual or a company that provides E507 active pharmaceutical ingredient (API) or E507 finished formulations upon request. The E507 suppliers may include E507 API manufacturers, exporters, distributors and traders.
click here to find a list of E507 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E507 DMF (Drug Master File) is a document detailing the whole manufacturing process of E507 active pharmaceutical ingredient (API) in detail. Different forms of E507 DMFs exist exist since differing nations have different regulations, such as E507 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A E507 DMF submitted to regulatory agencies in the US is known as a USDMF. E507 USDMF includes data on E507's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The E507 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of E507 suppliers with USDMF on PharmaCompass.
