Amlodipine Besylate and Benazepril Hydrochloride - amlodipine besylate and benazepril hydrochloride
Navigation: NDC > Supplier starting with: C > CLINICAL SOLUTIONS WHOLESALE| Field | Value |
|---|---|
| NDC Code: | 58118-2271 |
| Proprietary Name: | Amlodipine Besylate and Benazepril Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | amlodipine besylate and benazepril hydrochloride |
| Dosage Form: | CAPSULE |
| Method: | ORAL |
| Original Marketing Date: | 03-03-1995 |
| Category Name: | NDA AUTHORIZED GENERIC |
| Application Number: | NDA020364 |
| Labeler: | CLINICAL SOLUTIONS WHOLESALE |
| Substance Name: | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Active Numerator Strength: | 2.5; 10 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| DEA Schedule: |