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

U.S. FDA Requirements: Metolazone

Pharmaceutical / Drug Definition : Inhibits electrolyte reabsorption from ascending loop of Henle and decreases reabsorption of sodium and potassium in distal renal tubules, increasing plasma osmotic pressure and promoting diuresis

In the United States, Metolazone is regulated by the U.S. Food and Drug Administration (FDA). FDA has specific requirements regarding the registration and listing of Metolazone.

Registrar Corp assists Metolazone companies with:

  • FDA Registration Metolazone
  • FDA Listing Metolazone
  • FDA Label Requirements and Exceptions Metolazone
  • FDA Import Information Metolazone
  • FDA Detentions Metolazone (Metolazone Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Metolazone (Metolazone Suppliers)
       - Processors Metolazone
       - Repackers Metolazone
       - Relabelers Metolazone
       - Exporters Metolazone
       - Importers Metolazone
For more information about Metolazone, simply click below:

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U.S. FDA Regulations:

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

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
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