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Lotrel

NDC 0078-0379 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameamlodipine besylate and benazepril hydrochloride
Labeler / ManufacturerNovartis Pharmaceuticals Corporation
Marketing categoryNew Drug Application (innovator) · App NDA020364
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
BENAZEPRIL HYDROCHLORIDE (40 mg/1)
Marketing started19950303
Marketing ended20260930
Package count1

External sources

Source: openFDA. Public-domain (CC0).