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HomeDrugsU.S. FDA Active Pharmaceutical Ingredients (API)API Examples › U.S. FDA Regulations: Hydrochlorothiazide

U.S. FDA Requirements: Hydrochlorothiazide

Pharmaceutical / Drug Definition : Increases sodium and water excretion by inhibiting sodium reabsorption in distal tubules; promotes excretion of chloride, potassium, magnesium, and bicarbonate. Also may produce arteriolar dilation, reducing blood pressure.

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  • FDA Registration Hydrochlorothiazide
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  • FDA Label Requirements and Exceptions Hydrochlorothiazide
  • FDA Import Information Hydrochlorothiazide
  • FDA Detentions Hydrochlorothiazide (Hydrochlorothiazide Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Hydrochlorothiazide (Hydrochlorothiazide Suppliers)
       - Processors Hydrochlorothiazide
       - Repackers Hydrochlorothiazide
       - Relabelers Hydrochlorothiazide
       - Exporters Hydrochlorothiazide
       - Importers Hydrochlorothiazide
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U.S. FDA Regulations:

U.S. FDA Regulation: 21 C.F.R. Part 207


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