Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
EDQM
0
USP
0
JP
0
Others
0
Australia
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
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]NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]VMF
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
VMF Number : 6476
Submission : 2022-06-22
Status :
Type : II
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Listed Suppliers
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Phenylpropanolamine Hydrochloride
About the Company : Malladi Drugs & Pharmaceuticals Ltd was founded in 1980 by microbiologist Mr. M L N Sastry. Within a few years, Malladi established itself as a leader in manufacturing ephedrine an...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Phenylpropanolamine Hydrochloride
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
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
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]Canada
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
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]Microlex e.U
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Coating Systems & Additives
Lubricants & Glidants
Film Formers & Plasticizers
Fillers, Diluents & Binders
Direct Compression
Emulsifying Agents
Thickeners and Stabilizers
API Stability Enhancers
Topical
Co-Processed Excipients
Granulation
Digital Content
NEWS #PharmaBuzz
Global Sales Information
Market Place
ABOUT THIS PAGE
36
PharmaCompass offers a list of Phenylpropanolamine Hydrochloride 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 Phenylpropanolamine Hydrochloride manufacturer or Phenylpropanolamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenylpropanolamine Hydrochloride manufacturer or Phenylpropanolamine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Phenylpropanolamine Hydrochloride API Price utilized in the formulation of products. Phenylpropanolamine Hydrochloride API Price is not always fixed or binding as the Phenylpropanolamine Hydrochloride Price is obtained through a variety of data sources. The Phenylpropanolamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2-amino-1-phenylpropan-1-ol;hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-amino-1-phenylpropan-1-ol;hydrochloride, including repackagers and relabelers. The FDA regulates 2-amino-1-phenylpropan-1-ol;hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-amino-1-phenylpropan-1-ol;hydrochloride 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 2-amino-1-phenylpropan-1-ol;hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 2-amino-1-phenylpropan-1-ol;hydrochloride supplier is an individual or a company that provides 2-amino-1-phenylpropan-1-ol;hydrochloride active pharmaceutical ingredient (API) or 2-amino-1-phenylpropan-1-ol;hydrochloride finished formulations upon request. The 2-amino-1-phenylpropan-1-ol;hydrochloride suppliers may include 2-amino-1-phenylpropan-1-ol;hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of 2-amino-1-phenylpropan-1-ol;hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 2-amino-1-phenylpropan-1-ol;hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of 2-amino-1-phenylpropan-1-ol;hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of 2-amino-1-phenylpropan-1-ol;hydrochloride DMFs exist exist since differing nations have different regulations, such as 2-amino-1-phenylpropan-1-ol;hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 2-amino-1-phenylpropan-1-ol;hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. 2-amino-1-phenylpropan-1-ol;hydrochloride USDMF includes data on 2-amino-1-phenylpropan-1-ol;hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 2-amino-1-phenylpropan-1-ol;hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 2-amino-1-phenylpropan-1-ol;hydrochloride suppliers with USDMF 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 2-amino-1-phenylpropan-1-ol;hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 2-amino-1-phenylpropan-1-ol;hydrochloride 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 2-amino-1-phenylpropan-1-ol;hydrochloride 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 2-amino-1-phenylpropan-1-ol;hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 2-amino-1-phenylpropan-1-ol;hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 2-amino-1-phenylpropan-1-ol;hydrochloride suppliers with NDC on PharmaCompass.
2-amino-1-phenylpropan-1-ol;hydrochloride 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 2-amino-1-phenylpropan-1-ol;hydrochloride 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 2-amino-1-phenylpropan-1-ol;hydrochloride GMP manufacturer or 2-amino-1-phenylpropan-1-ol;hydrochloride GMP API supplier for your needs.
A 2-amino-1-phenylpropan-1-ol;hydrochloride CoA (Certificate of Analysis) is a formal document that attests to 2-amino-1-phenylpropan-1-ol;hydrochloride's compliance with 2-amino-1-phenylpropan-1-ol;hydrochloride specifications and serves as a tool for batch-level quality control.
2-amino-1-phenylpropan-1-ol;hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each 2-amino-1-phenylpropan-1-ol;hydrochloride 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.
2-amino-1-phenylpropan-1-ol;hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (2-amino-1-phenylpropan-1-ol;hydrochloride EP), 2-amino-1-phenylpropan-1-ol;hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-amino-1-phenylpropan-1-ol;hydrochloride USP).
