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1. Azo Dine
2. Azo Gesic
3. Azo Natural
4. Azo Standard
5. Azo-dine
6. Azo-gesic
7. Azo-natural
8. Azo-standard
9. Azodine
10. Azogesic
11. Azonatural
12. Azostandard
13. Baridium
14. Geridium
15. Hydrochloride, Phenazopyridine
16. Phenazo
17. Phenazopyridine
18. Prodium
19. Pyridiate
20. Pyridium
21. Re Azo
22. Re-azo
23. Reazo
24. Urogesic
25. Uti Relief
1. 136-40-3
2. Phenazopyridine Hcl
3. Pyridium
4. Urodine
5. Mallophene
6. Pyripyridium
7. Azomine
8. Bisteril
9. Diridone
10. Sedural
11. Suladyne
12. 3-phenylazo-2,6-diaminopyridine Hydrochloride
13. Phenazodine
14. Pyrazodine
15. Azodyne
16. Pirid
17. Phenylazo Tablets
18. Di-azo
19. Phenazopyridine.hcl
20. Pyridacil
21. Pyridiate
22. Uridinal
23. Nc 150
24. Phenazopyridinium Chloride
25. 3-(phenyldiazenyl)pyridine-2,6-diamine Hydrochloride
26. 2,6-pyridinediamine, 3-(phenylazo)-, Monohydrochloride
27. W 1655
28. Nci-c01672
29. 2,6-diamino-3-(phenylazo)pyridine Monohydrochloride
30. 2,6-diamino-3-phenylazopyridine Hydrochloride
31. Phenazopyridine (hydrochloride)
32. 2,6-pyridinediamine, 3-(2-phenyldiazenyl)-, Hydrochloride (1:1)
33. Nsc-1879
34. 3-phenyldiazenylpyridine-2,6-diamine;hydrochloride
35. Mls000069507
36. Pyri-pyridium
37. Chebi:71419
38. 0ewg668w17
39. 3-(phenylazo)-2,6-pyridinediamine Hydrochloride
40. Component Of Sulfid
41. Component Of Azotrex
42. Component Of Dolonil
43. Nc-150
44. Azosulfisox
45. Mallofeen
46. Nefrecil
47. Pyridivite
48. Pyrizin
49. Smr000058632
50. Urazium
51. Uriplex
52. Phenyl-idium
53. Azo-standard
54. Component Of Azo Gantanol
55. Dsstox_cid_1118
56. W-1655
57. 2,6-diamino-3-(phenylazo)pyridine Hydrochloride
58. Component Of Azo-mandelamine
59. Dsstox_rid_75950
60. Dsstox_gsid_21118
61. Thiosulfil-a Forte
62. Phenazopyridine M Hydrochloride
63. Phenyl-idium 200
64. Pyridene
65. Thiosulfil-a
66. 2, 3-(phenylazo)-, Monohydrochloride
67. Wln: T6nj Bz Cnunr & Fz & Gh
68. Ccris 497
69. Phenylazopyridine Hydrochloride
70. 3-phenylazo-2,6-diaminopyridine Monohydrochloride
71. Nsc227115
72. 3-(phenylazo)-2,6-diaminopyridine Hydrochloride
73. Pyridine,6-diamino-3-(phenylazo)-, Hydrochloride
74. Ncgc00018130-04
75. Nsc 1879
76. Cas-136-40-3
77. Einecs 205-243-8
78. Phenazopyridine Hydrochloride [usan]
79. Phenylazodiaminopyridine Hydrochloride
80. Mfcd00035347
81. Pyridine,6-diamino-3-(phenylazo)-, Monohydrochloride
82. 2,6-diamino-3-(phenylazo)-pyridine Hydrochloride
83. 3-[(e)-phenyldiazenyl]pyridine-2,6-diamine;hydrochloride
84. Phenylazo-.alpha.,.alpha.'-diaminopyridine Monohydrochloride
85. .beta.-phenylazo-.alpha.,.alpha.'-diaminopyridine Hydrochloride
86. Unii-0ewg668w17
87. Ai3-51273
88. Sr-05000001695
89. 3-(phenylazo)-2,6-pyridinediamine, Hydrochloride
90. Prestwick_158
91. Pyridine, 2,6-diamino-3-(phenylazo)-, Hydrochloride
92. Phenylazo-alpha,alpha'-diaminopyridine Monohydrochloride
93. Phenazopyridine Hydrochloride [usan:usp]
94. Opera_id_1284
95. Schembl19357
96. Mls001074123
97. Mls002222176
98. Spectrum1500473
99. Phenazopyridine Monohydrochloride
100. Chembl1201022
101. Chembl1606101
102. Dtxsid1021118
103. (e)-3-(phenyldiazenyl)pyridine-2,6-diamine Hydrochloride
104. 3-(2-phenyldiazen-1-yl)pyridine-2,6-diamine Hydrochloride
105. Nsc1879
106. Pyridine, 2,6-diamino-3-(phenylazo)-, Monohydrochloride
107. Hms1570g06
108. Hms1920f18
109. Pharmakon1600-01500473
110. Hy-b0985
111. Phenazopyridine Hydrochloride (usp)
112. Phenazopyridine Hydrochloride(usan)
113. Tox21_110829
114. Tox21_202153
115. Tox21_302738
116. Ccg-39935
117. Nsc757267
118. S4235
119. Akos015919909
120. Akos025401514
121. Tox21_110829_1
122. Ac-2036
123. Cs-4476
124. Ks-1427
125. Nsc-227115
126. Nsc-757267
127. Ncgc00018130-09
128. Ncgc00091334-01
129. Ncgc00091334-03
130. Ncgc00094755-01
131. Ncgc00094755-02
132. Ncgc00094755-03
133. Ncgc00094755-04
134. Ncgc00256528-01
135. Ncgc00259702-01
136. Phenazopyridine Hydrochloride [mi]
137. Phenazopyridine Hydrochloride [iarc]
138. B0022
139. Ft-0603345
140. Phenazopyridine Hydrochloride [mart.]
141. Phenazopyridine Hydrochloride [vandf]
142. Sw196469-3
143. Phenazopyridine Hydrochloride [usp-rs]
144. Phenazopyridine Hydrochloride [who-dd]
145. Bim-0051479.0001
146. C19290
147. D05450
148. D88590
149. Phenazopyridine Hydrochloride [orange Book]
150. Phenazopyridine Hydrochloride [usp Monograph]
151. Sr-05000001695-2
152. W-108251
153. Q27139594
154. Azo Gantanol Component Phenazopyridine Hydrochloride
155. Azo Gantrisin Component Phenazopyridine Hydrochloride
156. Phenazopyridine Hydrochloride Component Of Azo Gantanol
157. Phenazopyridine Hydrochloride Component Of Azo Gantrisin
158. 3-[(1e)-2-phenyldiazen-1-yl]pyridine-2,6-diamine Hydrochloride
159. Phenazopyridine Hydrochloride, Vetranal(tm), Analytical Standard
160. Phenazopyridine Hydrochloride, United States Pharmacopeia (usp) Reference Standard
| Molecular Weight | 249.70 g/mol |
|---|---|
| Molecular Formula | C11H12ClN5 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 2 |
| Exact Mass | 249.0781231 g/mol |
| Monoisotopic Mass | 249.0781231 g/mol |
| Topological Polar Surface Area | 89.6 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 237 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Phenazopyridine 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 Phenazopyridine manufacturer or Phenazopyridine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenazopyridine manufacturer or Phenazopyridine supplier.
PharmaCompass also assists you with knowing the Phenazopyridine API Price utilized in the formulation of products. Phenazopyridine API Price is not always fixed or binding as the Phenazopyridine Price is obtained through a variety of data sources. The Phenazopyridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Uriplex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uriplex, including repackagers and relabelers. The FDA regulates Uriplex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uriplex 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 Uriplex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Uriplex supplier is an individual or a company that provides Uriplex active pharmaceutical ingredient (API) or Uriplex finished formulations upon request. The Uriplex suppliers may include Uriplex API manufacturers, exporters, distributors and traders.
click here to find a list of Uriplex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Uriplex DMF (Drug Master File) is a document detailing the whole manufacturing process of Uriplex active pharmaceutical ingredient (API) in detail. Different forms of Uriplex DMFs exist exist since differing nations have different regulations, such as Uriplex USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Uriplex DMF submitted to regulatory agencies in the US is known as a USDMF. Uriplex USDMF includes data on Uriplex's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Uriplex USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Uriplex suppliers with USDMF on PharmaCompass.
A Uriplex written confirmation (Uriplex WC) is an official document issued by a regulatory agency to a Uriplex manufacturer, verifying that the manufacturing facility of a Uriplex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Uriplex APIs or Uriplex finished pharmaceutical products to another nation, regulatory agencies frequently require a Uriplex WC (written confirmation) as part of the regulatory process.
click here to find a list of Uriplex 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 Uriplex as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Uriplex 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 Uriplex 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 Uriplex and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Uriplex NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Uriplex suppliers with NDC on PharmaCompass.
Uriplex 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 Uriplex 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 Uriplex GMP manufacturer or Uriplex GMP API supplier for your needs.
A Uriplex CoA (Certificate of Analysis) is a formal document that attests to Uriplex's compliance with Uriplex specifications and serves as a tool for batch-level quality control.
Uriplex CoA mostly includes findings from lab analyses of a specific batch. For each Uriplex 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.
Uriplex may be tested according to a variety of international standards, such as European Pharmacopoeia (Uriplex EP), Uriplex JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Uriplex USP).
