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

U.S. FDA Requirements: Levalbuterol Hydrochloride

Pharmaceutical / Drug Definition : Binds to beta2-adrenergic receptors on bronchial cell membrane, stimulating the intracellular enzyme adenylate cyclase to convert adenosine triphosphate to cyclic-3′,5′-adenosine monophosphate. This action relaxes smooth muscles, dilates bronchioles, and increases diuresis.

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




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U.S. FDA Regulations:

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


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