Synopsis
0
JDMF
0
EU WC
0
VMF
0
Canada
0
Australia
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CEP/COS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
INTERMEDIATE SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Boai NKY Pharmaceuticals Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ACG Worldwide
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Alcedo Pharmachem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ashland
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DFE Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ideal Cures Pvt Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ingredion Pharma Solutions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kerry
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Lonza Capsugel
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Microlex e.U
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Novo Excipients
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharmatrans-Sanaq
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pluviaendo
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Prachin Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Qualicaps
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Roquette
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Seppic
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Welltone Material Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sigachi Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Silverline Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ulanqab Kema New Material
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
Direct Compression
Disintegrants & Superdisintegrants
Thickeners and Stabilizers
Granulation
Lubricants & Glidants
Coating Systems & Additives
Co-Processed Excipients
Solubilizers
Chewable & Orodispersible Aids
Empty Capsules
Controlled & Modified Release
Film Formers & Plasticizers
Taste Masking
Emulsifying Agents
Coloring Agents
Parenteral
API Stability Enhancers
Topical
Rheology Modifiers
Digital Content
NEWS #PharmaBuzz
Global Sales Information
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
86
PharmaCompass offers a list of Dihydrocodeine Tartrate 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 Dihydrocodeine Tartrate manufacturer or Dihydrocodeine Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dihydrocodeine Tartrate manufacturer or Dihydrocodeine Tartrate supplier.
PharmaCompass also assists you with knowing the Dihydrocodeine Tartrate API Price utilized in the formulation of products. Dihydrocodeine Tartrate API Price is not always fixed or binding as the Dihydrocodeine Tartrate Price is obtained through a variety of data sources. The Dihydrocodeine Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DF 118 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DF 118, including repackagers and relabelers. The FDA regulates DF 118 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DF 118 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 DF 118 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DF 118 supplier is an individual or a company that provides DF 118 active pharmaceutical ingredient (API) or DF 118 finished formulations upon request. The DF 118 suppliers may include DF 118 API manufacturers, exporters, distributors and traders.
click here to find a list of DF 118 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DF 118 DMF (Drug Master File) is a document detailing the whole manufacturing process of DF 118 active pharmaceutical ingredient (API) in detail. Different forms of DF 118 DMFs exist exist since differing nations have different regulations, such as DF 118 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DF 118 DMF submitted to regulatory agencies in the US is known as a USDMF. DF 118 USDMF includes data on DF 118's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DF 118 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DF 118 suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a DF 118 Drug Master File in Korea (DF 118 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DF 118. The MFDS reviews the DF 118 KDMF as part of the drug registration process and uses the information provided in the DF 118 KDMF to evaluate the safety and efficacy of the drug.
After submitting a DF 118 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their DF 118 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of DF 118 suppliers with KDMF on PharmaCompass.
A DF 118 CEP of the European Pharmacopoeia monograph is often referred to as a DF 118 Certificate of Suitability (COS). The purpose of a DF 118 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DF 118 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DF 118 to their clients by showing that a DF 118 CEP has been issued for it. The manufacturer submits a DF 118 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DF 118 CEP holder for the record. Additionally, the data presented in the DF 118 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DF 118 DMF.
A DF 118 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DF 118 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of DF 118 suppliers with CEP (COS) 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 DF 118 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for DF 118 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 DF 118 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 DF 118 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DF 118 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of DF 118 suppliers with NDC on PharmaCompass.
DF 118 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of DF 118 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right DF 118 GMP manufacturer or DF 118 GMP API supplier for your needs.
A DF 118 CoA (Certificate of Analysis) is a formal document that attests to DF 118's compliance with DF 118 specifications and serves as a tool for batch-level quality control.
DF 118 CoA mostly includes findings from lab analyses of a specific batch. For each DF 118 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
DF 118 may be tested according to a variety of international standards, such as European Pharmacopoeia (DF 118 EP), DF 118 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DF 118 USP).
