Azuranit
Category
Azuranit Brand names, Azuranit Analogs
Azuranit Brand Names Mixture
Tritec (ranitidine bismuth citrate salt)
Azuranit Chemical_Formula
C13H22N4O3S
Azuranit RX_link
http://www.rxlist.com/cgi/generic2/ranitbc.htm
Azuranit fda sheet
Azuranit msds (material safety sheet)
Azuranit Synthesis Reference
B. J. Price et al., U.S. Pat. 4,128,658 (1978)
Azuranit Molecular Weight
314.405 g/mol
Azuranit Melting Point
69-70 oC
Azuranit H2O Solubility
24.7 mg/mL
Azuranit State
Solid
Azuranit LogP
1.93
Azuranit Dosage Forms
Capsule; Liquid; Solution; Tablet; Syrup
Azuranit Indication
Used in the treatment of peptic ulcer disease (PUD), dyspepsia, stress ulcer prophylaxis, and gastroesophageal reflux disease (GERD).
Azuranit Pharmacology
Ranitidine is a histamine H2-receptor antagonist similar to cimetidine and famotidine. An H2-receptor antagonist, often shortened to H2 antagonist, is a drug used to block the action of histamine on parietal cells in the stomach, decreasing acid production by these cells. These drugs are used in the treatment of dyspepsia, however their use has waned since the advent of the more effective proton pump inhibitors. Like the H1-antihistamines, the H2 antagonists are inverse agonists rather than true receptor antagonists.
Azuranit Absorption
Approximately 50% bioavailability orally.
Azuranit Toxicity
LD50=77mg/kg (orally in mice). Symptoms of overdose include muscular tremors, vomiting, and rapid respiration.
Azuranit Patient Information
PATIENT INFORMATION
Phenylketonurics: ZANTAC 25 EFFERdose Tablets contain phenylalanine 2.81 mg per 25 mg of ranitidine. ZANTAC 150 EFFERdose Tablets
contain phenylalanine 16.84 mg per 150 mg of ranitidine. ZANTAC EFFERdose Tablets should not be chewed, swallowed whole, or dissolved
on the tongue.
Azuranit Organisms Affected
Humans and other mammals
