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1. 1027-30-1
2. D-benzphetamine Hydrochloride
3. N-benzyl-n-methyl-1-phenylpropan-2-amine;hydrochloride
4. N-benzyl-n-methyl-1-phenyl-2-propanamine Hydrochloride
5. Didrex (tn)
6. N-benzyl-n,alpha-dimethylphenethylamine Hydrochloride
7. Dtxsid70908004
8. N,alpha-dimethyl-n-(phenylmethyl)benzeneethanamine Hydrochloride
9. Nsc10937
10. Benzeneethanamine, N,alpha-dimethyl-n-(phenylmethyl)-, Hydrochloride (1:1)
11. 5411-22-3 (hcl)
12. Ft-0662617
13. Ft-0662619
14. D07515
15. N-benzyl-n-methyl-1-phenylpropan-2-amine--hydrogen Chloride (1/1)
16. Benzeneethanamine,.alpha.-dimethyl-n-(phenylmethyl)-, Hydrochloride, (+)-
Molecular Weight | 275.8 g/mol |
---|---|
Molecular Formula | C17H22ClN |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 5 |
Exact Mass | 275.1440774 g/mol |
Monoisotopic Mass | 275.1440774 g/mol |
Topological Polar Surface Area | 3.2 Ų |
Heavy Atom Count | 19 |
Formal Charge | 0 |
Complexity | 214 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
1 of 4 | |
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Drug Name | Benzphetamine hydrochloride |
PubMed Health | Benzphetamine (By mouth) |
Drug Classes | Appetite Suppressant, Centrally Acting |
Drug Label | DIDREX Tablets contain the anorectic agent benzphetamine hydrochloride. Benzphetamine hydrochloride is a white crystalline powder readily soluble in water and 95% ethanol. The chemical name for benzphetamine hydrochloride is d-N,-Dimethyl-N-(phenyl... |
Active Ingredient | Benzphetamine hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 25mg; 50mg |
Market Status | Prescription |
Company | Emcure Pharms; Paddock; Kvk Tech; Tedor Pharm; Mallinckrodt; Mikart; Impax Labs |
2 of 4 | |
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Drug Name | Didrex |
Drug Label | DIDREX Tablets contain the anorectic agent benzphetamine hydrochloride. Benzphetamine hydrochloride is a white crystalline powder readily soluble in water and 95% ethanol. The chemical name for benzphetamine hydrochloride is d-N,-Dimethyl-N-(phenyl... |
Active Ingredient | Benzphetamine hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 50mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
3 of 4 | |
---|---|
Drug Name | Benzphetamine hydrochloride |
PubMed Health | Benzphetamine (By mouth) |
Drug Classes | Appetite Suppressant, Centrally Acting |
Drug Label | DIDREX Tablets contain the anorectic agent benzphetamine hydrochloride. Benzphetamine hydrochloride is a white crystalline powder readily soluble in water and 95% ethanol. The chemical name for benzphetamine hydrochloride is d-N,-Dimethyl-N-(phenyl... |
Active Ingredient | Benzphetamine hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 25mg; 50mg |
Market Status | Prescription |
Company | Emcure Pharms; Paddock; Kvk Tech; Tedor Pharm; Mallinckrodt; Mikart; Impax Labs |
4 of 4 | |
---|---|
Drug Name | Didrex |
Drug Label | DIDREX Tablets contain the anorectic agent benzphetamine hydrochloride. Benzphetamine hydrochloride is a white crystalline powder readily soluble in water and 95% ethanol. The chemical name for benzphetamine hydrochloride is d-N,-Dimethyl-N-(phenyl... |
Active Ingredient | Benzphetamine hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 50mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Benzphetamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzphetamine, including repackagers and relabelers. The FDA regulates Benzphetamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzphetamine 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 Benzphetamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benzphetamine supplier is an individual or a company that provides Benzphetamine active pharmaceutical ingredient (API) or Benzphetamine finished formulations upon request. The Benzphetamine suppliers may include Benzphetamine API manufacturers, exporters, distributors and traders.
click here to find a list of Benzphetamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Benzphetamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Benzphetamine active pharmaceutical ingredient (API) in detail. Different forms of Benzphetamine DMFs exist exist since differing nations have different regulations, such as Benzphetamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Benzphetamine DMF submitted to regulatory agencies in the US is known as a USDMF. Benzphetamine USDMF includes data on Benzphetamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Benzphetamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Benzphetamine suppliers with USDMF on PharmaCompass.
A Benzphetamine written confirmation (Benzphetamine WC) is an official document issued by a regulatory agency to a Benzphetamine manufacturer, verifying that the manufacturing facility of a Benzphetamine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Benzphetamine APIs or Benzphetamine finished pharmaceutical products to another nation, regulatory agencies frequently require a Benzphetamine WC (written confirmation) as part of the regulatory process.
click here to find a list of Benzphetamine suppliers with Written Confirmation (WC) 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 Benzphetamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Benzphetamine 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 Benzphetamine 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 Benzphetamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Benzphetamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Benzphetamine suppliers with NDC on PharmaCompass.
Benzphetamine 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 Benzphetamine 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 Benzphetamine GMP manufacturer or Benzphetamine GMP API supplier for your needs.
A Benzphetamine CoA (Certificate of Analysis) is a formal document that attests to Benzphetamine's compliance with Benzphetamine specifications and serves as a tool for batch-level quality control.
Benzphetamine CoA mostly includes findings from lab analyses of a specific batch. For each Benzphetamine 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.
Benzphetamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Benzphetamine EP), Benzphetamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Benzphetamine USP).
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