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Uniretic - moexipril hydrochloride and hydrochlorothiazide

Navigation: NDC > Supplier starting with: U > UCB, INC.
Field Value
NDC Code: 0091-3725
Proprietary Name: Uniretic
Suffix:
Non-Proprietary Name: moexipril hydrochloride and hydrochlorothiazide
Dosage Form: TABLET, FILM COATED
Method: ORAL
Original Marketing Date: 15-09-1997
Category Name: NDA
Application Number: NDA020729
Labeler: UCB, INC.
Substance Name: HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
Active Numerator Strength: 25; 15
Active Ingredient Unit: mg/1; mg/1
Pharm Classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]
DEA Schedule: