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Moexipril Hydrochloride and Hydrochlorothiazide - Moexipril Hydrochloride and Hydrochlorothiazide

Navigation: NDC > Supplier starting with: P > PADDOCK LABORATORIES, INC.
Field Value
NDC Code: 0574-0133
Proprietary Name: Moexipril Hydrochloride and Hydrochlorothiazide
Suffix:
Non-Proprietary Name: Moexipril Hydrochloride and Hydrochlorothiazide
Dosage Form: TABLET, COATED
Method: ORAL
Original Marketing Date: 01-07-2009
Category Name: ANDA
Application Number: ANDA090096
Labeler: PADDOCK LABORATORIES, INC.
Substance Name: HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
Active Numerator Strength: 12.5; 7.5
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: