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Lotensin - Benazepril Hydrochloride

Navigation: NDC > Supplier starting with: N > NOVARTIS PHARMACEUTICALS CORPORATION
Field Value
NDC Code: 0078-0449
Proprietary Name: Lotensin
Suffix:
Non-Proprietary Name: Benazepril Hydrochloride
Dosage Form: TABLET
Method: ORAL
Original Marketing Date: 25-06-1991
End of Marketing: 01-02-2016
Category Name: NDA
Application Number: NDA019851
Labeler: NOVARTIS PHARMACEUTICALS CORPORATION
Substance Name: BENAZEPRIL HYDROCHLORIDE
Active Numerator Strength: 20
Active Ingredient Unit: mg/1
Pharm Classes: Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
DEA Schedule: