Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 013553
Company: NOVARTIS
Company: NOVARTIS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
ESIMIL | GUANETHIDINE MONOSULFATE; HYDROCHLOROTHIAZIDE | 10MG;25MG | TABLET;ORAL | Discontinued | None | No | No |