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1. Dexatrim
2. Hydrochloride, Phenylpropanolamine
3. Norephedrine
4. Phenylpropanolamine
5. Phenylpropanolamine Hydrochloride
6. Prolamine
7. Propagest
8. Triaminic Dm
1. Phenylpropanolamine Hydrochloride
2. (+)-phenylpropanolamine Hydrochloride
3. 40626-29-7
4. Phenylpropanolamine Hydrochloride, (+)-
5. 184m412sjh
6. Dl-norephedrine Hydrochloride
7. (1s,2r)-2-amino-1-phenylpropan-1-ol Hydrochloride
8. 154-41-6
9. Dsstox_cid_5896
10. D-norephedrine Hydrochloride
11. Dsstox_rid_77964
12. Dsstox_gsid_25896
13. (+)-norephedrine Hydrochloride
14. Unii-184m412sjh
15. (1s,2r)-norephedrine Hydrochloride
16. Norephedrine, Hydrochloride, (+)-
17. Einecs 255-008-9
18. (1s,2r)-(+)-norephedrine Hydrochloride
19. Dl-norephedrinhydrochlorid
20. Ncgc00016416-01
21. Cas-154-41-6
22. Schembl16986
23. 1s,2r-phenylpropanolamine Hydrochloride
24. Chembl3189135
25. Dtxsid2025896
26. Tox21_110431
27. Tox21_110431_1
28. Ccg-212747
29. Dl-norephedrine Hydrochloride, >=99%
30. Ncgc00274057-01
31. D-phenylpropanolamine Hydrochloride
32. (1s, 2r)-(+)-norephedrine Hydrochloride
33. (1s,2r)-2-amino-1-phenylpropan-1-ol;hydrochloride
34. D-(+)-norephedrine Hydrochloride, >=98.0% (at)
35. Q27251969
36. Dl-norephedrine Hydrochloride, Sigma Reference Standard
37. Phenylpropanolamine (+)-form Hydrochloride [mi]
38. (s-(r*,s*))-alpha-(1-aminoethyl)benzyl Alcohol Hydrochloride
39. Benzenemethanol, .alpha.-((1r)-1-aminoethyl)-, Hydrochloride (1:1), (.alpha.s)-
40. Phenylpropanolamine Hydrochloride, European Pharmacopoeia (ep) Reference Standard
41. Phenylpropanolamine Hydrochloride, United States Pharmacopeia (usp) Reference Standard
42. (+/-)-phenylpropanolamine Hydrochloride Solution, 1.0 Mg/ml In Methanol (as Free Base), Ampule Of 1 Ml, Certified Reference Material
Molecular Weight | 187.66 g/mol |
---|---|
Molecular Formula | C9H14ClNO |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 2 |
Exact Mass | 187.0763918 g/mol |
Monoisotopic Mass | 187.0763918 g/mol |
Topological Polar Surface Area | 46.2 Ų |
Heavy Atom Count | 12 |
Formal Charge | 0 |
Complexity | 110 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 2 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
Nasal Decongestants
Drugs designed to treat inflammation of the nasal passages, generally the result of an infection (more often than not the common cold) or an allergy related condition, e.g., hay fever. The inflammation involves swelling of the mucous membrane that lines the nasal passages and results in inordinate mucus production. The primary class of nasal decongestants are vasoconstrictor agents. (From PharmAssist, The Family Guide to Health and Medicine, 1993) (See all compounds classified as Nasal Decongestants.)
Sympathomimetics
Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters. (See all compounds classified as Sympathomimetics.)
Adrenergic alpha-Agonists
Drugs that selectively bind to and activate alpha adrenergic receptors. (See all compounds classified as Adrenergic alpha-Agonists.)
Appetite Depressants
Agents that are used to suppress appetite. (See all compounds classified as Appetite Depressants.)
ABOUT THIS PAGE
A Monydrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monydrin, including repackagers and relabelers. The FDA regulates Monydrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monydrin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Monydrin supplier is an individual or a company that provides Monydrin active pharmaceutical ingredient (API) or Monydrin finished formulations upon request. The Monydrin suppliers may include Monydrin API manufacturers, exporters, distributors and traders.
Monydrin 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 Monydrin 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 Monydrin GMP manufacturer or Monydrin GMP API supplier for your needs.
A Monydrin CoA (Certificate of Analysis) is a formal document that attests to Monydrin's compliance with Monydrin specifications and serves as a tool for batch-level quality control.
Monydrin CoA mostly includes findings from lab analyses of a specific batch. For each Monydrin 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.
Monydrin may be tested according to a variety of international standards, such as European Pharmacopoeia (Monydrin EP), Monydrin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Monydrin USP).
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