Visitor Monitoring Drug Details: TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
 
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Drug Details

Drug Name: TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No: (NDA) 019434
Active Ingredient(s): CIMETIDINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: October 31, 1985
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER CIMETIDINE HYDROCHLORIDEEQ 6MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None


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