Amlodipine Besylate and Benazepril Hydrochloride - Amlodipine Besylate and Benazepril Hydrochloride
Navigation: NDC > Supplier starting with: A > AUROBINDO PHARMA LIMITED| Field | Value |
|---|---|
| NDC Code: | 65862-584 |
| Proprietary Name: | Amlodipine Besylate and Benazepril Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Amlodipine Besylate and Benazepril Hydrochloride |
| Dosage Form: | CAPSULE |
| Method: | ORAL |
| Original Marketing Date: | 05-09-2012 |
| Category Name: | ANDA |
| Application Number: | ANDA202239 |
| Labeler: | AUROBINDO PHARMA LIMITED |
| Substance Name: | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Active Numerator Strength: | 5; 20 |
| 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: |