Products

What will AGI do for Amiloride?

This classification denotes a potassium-sparing diuretic and intercalating agent with the molecular formula C6H8ClN7O, a preparation that US FDA regulates as an active ingredient or moiety under Unique Ingredient Identifier 7DZO8EB0Z3, chemically known as 3,5-diamino-n-(aminoiminomethyl)-6-chloropyrazinecarboxamide but generally known as amiloride, which bears US NIH Compound Identifier 16231. Amiloride most often comes in caproate, chloride, hydrochloride, hydrochloride dihydrate, and hydrochloride-hydrochlorothiazide forms. European Medicines Agency schedules Amiloride in its eXtended EudraVigilance Medicinal Product Dictionary or XEVMPD under Index SUB05433MIG. The term AMILORIDE is an International Non-Proprietary Name or INN (see WHO INN reference publication, Volume 22, No. 10, 1968, List 8). World Health Organization schedules amiloride in its Anatomical Therapeutic Chemical (ATC) Classification. AMILORIDE is scheduled in the U.S. International Trade Commission's Harmonized Tariff System (HTS) Pharmaceutical Appendix. Most nations schedule Amiloride under HS 29339990 and SITC 51577. As of Q4 2014, AMILORIDE remains the US FDA Preferred Term for this commodity. Amiloride bears US NLM identifiers UMLS ID C0002502 and NCI Concept Code C61633. SMILES: C1(C(NC(C(N1)CL)N)N)C(=O)NC(=N)N.