Lotensin - Benazepril Hydrochloride
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Field |
Value |
NDC Code: |
54868-3690 |
Proprietary Name: |
Lotensin |
Suffix: |
|
Non-Proprietary Name: |
Benazepril Hydrochloride |
Dosage Form: |
TABLET |
Method: |
ORAL |
Original Marketing Date: |
30-12-1996 |
Category Name: |
NDA |
Application Number: |
NDA019851 |
Labeler: |
PHYSICIANS TOTAL CARE, INC. |
Substance Name: |
BENAZEPRIL HYDROCHLORIDE |
Active Numerator Strength: |
5 |
Active Ingredient Unit: |
mg/1 |
Pharm Classes: |
Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
DEA Schedule: |
|