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LotensinDrug - Lotensin The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Benazepril Hydrochloride
Strength -
20MG
Applicant -
NOVARTIS
New Drug Application (NDA) Number -
019851
Product Number -
003
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Jun 25, 1991
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Novartis Pharmaceuticals Corp
Lotensin
Benazepril Hcl 5mg Tablet; Oral
Lotensin 10mg Tablet; Oral Lotensin 20mg Tablet; Oral Benazepril Hcl 10mg Tablet; Oral Benazepril Hcl 20mg Tablet; Oral Benazepril Hcl 40mg Tablet; Oral Benazepril Hcl 5mg Tablet; Oral Benazepril Hcl 10mg Tablet; Oral Benazepril Hcl 20mg Tablet; Oral Benazepril Hcl 40mg Tablet; Oral NewDrugInformation |