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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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Wholesale distributors and TMOPs, are instructed to immediately stop distribution, quarantine all remaining products in their control, and return the recalled product to GSMS, Inc. The consignees are also instructed to provide their customers, i. pharmacies and consumers, a copy of GSMS, Inc. s recall notification, recall response form, and letter to prilosec 150 mg, patients, and caregivers.Over-the-counter and prescription Zantac have different instructions for use.
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Psychiatric Medications Ranitidine 20mg Valiuma common anti-anxiety drug, can cause a false-positive result for alcohol.or more information visit the official Government of Canada recall notice: ealthycanadians. c.
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