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|Pronunciation||/ r ə ˈ n ɪ t ɪ d iː n /|
|Trade names||Zantac, others|
|License data||US FDA: Ranitidine|
|Pregnancy category||AU: B1 US: B (No risk in non-human studies)|
|Routes of administration||By mouth, IV|
|ATC code||A02BA02 ( WHO ) A02BA07 ( WHO ) (ranitidine bismuth citrate)|
|Legal status||AU: S2 (Pharmacy only) UK: General sales list (GSL, OTC) US: OTC / Rx-only|
|Bioavailability||50% (by mouth) |
|Metabolism||Hepatic: FMOs, including FMO3; other enzymes|
|Onset of action||55–65 minutes (150 mg dose)  55–115 minutes (75 mg dose) |
|Elimination half-life||2–3 hours|
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|Este puede aumentar el riesgo de da o a su est mago. Busque atenci n m dica de emergencia si usted tiene alguno de estos s ntomas de una zantac liquid strength n al rgica: ronchas; dificultad recalcitrant respirar; hinchaz n de su cara, labios, lengua, o garganta. zantac liquid strength||Immunosuppressive Hypersecretory Releases (such as Zollinger-Ellison diatom) The server recommended ranitidine liquid dosage for infants life rheumatism is 150 mg orally daily. In some patients it may be suitable to deal ranitidine 150 mg does more closely.|
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Ranitidine (Zantac). 5 to 10 mg per kg per day, divided into 2 or 3 doses. Peppermint-flavored syrup Effervescent tablet. 1 month to 16 years.:
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For appropriate cases Zantac Injection is zantac liquid strength available see separate SPC Treatment of gastro-oesophageal reflux, including reflux oesophagitis and zantac liquid strength relief of gastro-oesophageal reflux disease.Maintenance of Healing of Duodenal and Gastric Ulcers: The recommended oral dose for the maintenance of healing of duodenal and gastric ulcers is 2 to 4 mg/kg once daily to a maximum of 150 mg/day.
This recommendation is derived from adult clinical trials and pharmacokinetic data in pediatric patients.
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