Amlodipine and Benazepril Hydrochloride (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Amlodipine and Benazepril Hydrochloride drug offered from Teva Pharmaceuticals USA, Inc.. This Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Teva Pharmaceuticals USA, Inc. |
| NON-PROPRIETARY NAME: | Amlodipine and Benazepril Hydrochloride |
| SUBSTANCE NAME: | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2011-07-20 |
| END MARKETING DATE: | 0000-00-00 |
Amlodipine and Benazepril Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Amlodipine and Benazepril Hydrochloride from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5; 40(mg/1; mg/1) |
| START MARKETING DATE: | 2011-07-20 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0093-7670_a804a97e-d1e0-411b-b075-557ac09684c0 |
| PRODUCT NDC: | 0093-7670 |
| APPLICATION NUMBER: | ANDA077179 |
Other AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
