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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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- Zantac other name: azantac, bismo-ranit, novo-ranitidine, nu-ranit, pylorid, raniplex, ranitic, ranitidina, ranitidinum, rantec, zaedoc, zantic
- Active substances: ranitidine
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As a result, Zantac and its generic equivalents are being pulled from zantac manufacturers coupon as part of a nationwide, voluntary recall. The recall has so far only listed tablet or capsule dosage forms, not the liquid.Due to inconsistencies in preliminary test results of the active ingredient used in the U. products, Sanofi has made the decision to conduct the voluntary recall as the investigation continues.
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The company is committed to transparency and will continue to communicate results with health authorities from the ongoing testing, and work with them to make informed decisions based on available data and evidence.
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