Esimil

NDA 13553, held by Novartis. Guanethidine Monosulfate; Hydrochlorothiazide.

As of Nov 13, 2026, NDA 13553 (Esimil), held by Novartis, was not approved, with 0 approved supplements and 0 published complete response letters.

• First approved: Not approved
• Supplements approved: 0
• Complete response letters: 0

Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters