Lotensin - Benazepril Hydrochloride
Navigation: NDC > Supplier starting with: P > PD RX PHARMACEUTICALS, INC.| Field | Value |
|---|---|
| NDC Code: | 55289-086 |
| Proprietary Name: | Lotensin |
| Suffix: | |
| Non-Proprietary Name: | Benazepril Hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 25-06-1991 |
| Category Name: | NDA |
| Application Number: | NDA019851 |
| Labeler: | PD RX PHARMACEUTICALS, INC. |
| 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: |