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Lotensin HCT - benazepril hydrochloride and hydrochlorothiazide

Navigation: NDC > Supplier starting with: N > NOVARTIS PHARMACEUTICALS CORPORATION
Field Value
NDC Code: 0078-0452
Proprietary Name: Lotensin HCT
Suffix:
Non-Proprietary Name: benazepril hydrochloride and hydrochlorothiazide
Dosage Form: TABLET
Method: ORAL
Original Marketing Date: 30-05-1992
End of Marketing: 31-12-2014
Category Name: NDA
Application Number: NDA020033
Labeler: NOVARTIS PHARMACEUTICALS CORPORATION
Substance Name: BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Active Numerator Strength: 10; 12.5
Active Ingredient Unit: mg/1; mg/1
Pharm Classes: Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]
DEA Schedule: