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: |