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Lotrel - amlodipine besylate and benazepril hydrochloride

Navigation: NDC > Supplier starting with: N > NOVARTIS PHARMACEUTICALS CORPORATION
Field Value
NDC Code: 0078-0379
Proprietary Name: Lotrel
Suffix:
Non-Proprietary Name: amlodipine besylate and benazepril hydrochloride
Dosage Form: CAPSULE
Method: ORAL
Original Marketing Date: 03-03-1995
Category Name: NDA
Application Number: NDA020364
Labeler: NOVARTIS PHARMACEUTICALS CORPORATION
Substance Name: AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Active Numerator Strength: 10; 40
Active Ingredient Unit: mg/1; mg/1
Pharm Classes: Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
DEA Schedule: