Synopsis
0
CEP/COS
0
EU WC
0
NDC API
0
VMF
0
Australia
DRUG PRODUCT COMPOSITIONS0
US Patents
0
US Exclusivities
0
Health Canada Patents
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]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Drugs in Development
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
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine Forte
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 2000-11-28
Application Number : 63496
Regulatory Info : Cancelled
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1998-04-01
Application Number : 61783
Regulatory Info : Cancelled
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine Forte
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 2000-11-28
Application Number : 63498
Regulatory Info : Cancelled
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1991-06-01
Application Number : 58983
Regulatory Info : Cancelled
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1989-11-01
Application Number : 58496
Regulatory Info : Cancelled
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine Forte
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 2000-11-28
Application Number : 63497
Regulatory Info : Cancelled
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1991-06-01
Application Number : 58982
Regulatory Info : Cancelled
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength : 9500IU
Packaging :
Approval Date : 2021-06-02
Application Number : 86000
Regulatory Info : Cancelled
Registration Country : Spain
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Canada
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.8ml
Dosage Form : INJ
Dosage Strength : 7600iu/0.8ml
Packaging : 0.8X10iu/0.8ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 1.0ml
Dosage Form : INJ
Dosage Strength : 9500iu/1ml
Packaging : 1X10iu/1ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.2ml
Dosage Form : INJ
Dosage Strength : 1900iu/0.2ml
Packaging : 0.2X10iu/0.2ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.3ml
Dosage Form : INJ
Dosage Strength : 2850iu/0.3ml
Packaging : 0.3X10iu/0.3ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.4ml
Dosage Form : INJ
Dosage Strength : 3800iu/0.4ml
Packaging : 0.4X10iu/0.4ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.6ml
Dosage Form : INJ
Dosage Strength : 5700iu/0.6ml
Packaging : 0.6X10iu/0.6ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - INJECTABLE;SUBCUTANEOUS - 10,000IU/M...DOSAGE - INJECTABLE;SUBCUTANEOUS - 10,000IU/ML (10,000IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 10,000IU/4...DOSAGE - INJECTABLE;SUBCUTANEOUS - 10,000IU/4ML (2,500IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 12,500IU/0...DOSAGE - INJECTABLE;SUBCUTANEOUS - 12,500IU/0.5ML (25,000IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 15,000IU/0...DOSAGE - INJECTABLE;SUBCUTANEOUS - 15,000IU/0.6ML (25,000IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 18,000IU/0...DOSAGE - INJECTABLE;SUBCUTANEOUS - 18,000IU/0.72ML (25,000IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 2,500IU/0....DOSAGE - INJECTABLE;SUBCUTANEOUS - 2,500IU/0.2ML (12,500IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 5,000IU/0....DOSAGE - INJECTABLE;SUBCUTANEOUS - 5,000IU/0.2ML (25,000IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 7,500IU/0....DOSAGE - INJECTABLE;SUBCUTANEOUS - 7,500IU/0.3ML (25,000IU/ML)
USFDA APPLICATION NUMBER - 20287
DOSAGE - INJECTABLE;SUBCUTANEOUS - 95,000IU/3...DOSAGE - INJECTABLE;SUBCUTANEOUS - 95,000IU/3.8ML (25,000IU/ML)
USFDA APPLICATION NUMBER - 20287
Related Excipient Companies
Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kirsch Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Parenteral
Topical
Solubilizers
Digital Content
DATA COMPILATION #PharmaFlow
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
38
PharmaCompass offers a list of Dalteparin sodium 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 Dalteparin sodium manufacturer or Dalteparin sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dalteparin sodium manufacturer or Dalteparin sodium supplier.
PharmaCompass also assists you with knowing the Dalteparin sodium API Price utilized in the formulation of products. Dalteparin sodium API Price is not always fixed or binding as the Dalteparin sodium Price is obtained through a variety of data sources. The Dalteparin sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Innohep manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Innohep, including repackagers and relabelers. The FDA regulates Innohep manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Innohep 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 Innohep manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Innohep supplier is an individual or a company that provides Innohep active pharmaceutical ingredient (API) or Innohep finished formulations upon request. The Innohep suppliers may include Innohep API manufacturers, exporters, distributors and traders.
click here to find a list of Innohep suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Innohep DMF (Drug Master File) is a document detailing the whole manufacturing process of Innohep active pharmaceutical ingredient (API) in detail. Different forms of Innohep DMFs exist exist since differing nations have different regulations, such as Innohep USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Innohep DMF submitted to regulatory agencies in the US is known as a USDMF. Innohep USDMF includes data on Innohep's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Innohep USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Innohep suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Innohep Drug Master File in Japan (Innohep JDMF) empowers Innohep API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Innohep JDMF during the approval evaluation for pharmaceutical products. At the time of Innohep JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Innohep suppliers with JDMF 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 Innohep Drug Master File in Korea (Innohep KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Innohep. The MFDS reviews the Innohep KDMF as part of the drug registration process and uses the information provided in the Innohep KDMF to evaluate the safety and efficacy of the drug.
After submitting a Innohep 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 Innohep API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Innohep suppliers with KDMF on PharmaCompass.
Innohep 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 Innohep 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 Innohep GMP manufacturer or Innohep GMP API supplier for your needs.
A Innohep CoA (Certificate of Analysis) is a formal document that attests to Innohep's compliance with Innohep specifications and serves as a tool for batch-level quality control.
Innohep CoA mostly includes findings from lab analyses of a specific batch. For each Innohep 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.
Innohep may be tested according to a variety of international standards, such as European Pharmacopoeia (Innohep EP), Innohep JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Innohep USP).
