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Amlodipine Besylate and Benazepril Hydrochloride
Amlodipine Besylate and Benazepril Hydrochloride - 65862-583-05 - (Amlodipine Besylate and Benazepril Hydrochloride)
Drug Information of Amlodipine Besylate and Benazepril Hydrochloride
| Product NDC: | 65862-583 |
| Proprietary Name: | Amlodipine Besylate and Benazepril Hydrochloride |
| Non Proprietary Name: | Amlodipine Besylate and Benazepril Hydrochloride |
| Active Ingredient(s): | 5; 10 mg/1; mg/1 & nbsp; Amlodipine Besylate and Benazepril Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amlodipine Besylate and Benazepril Hydrochloride
| Product NDC: | 65862-583 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202239 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120905 |
Package Information of Amlodipine Besylate and Benazepril Hydrochloride
| Package NDC: | 65862-583-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (65862-583-05) |
NDC Information of Amlodipine Besylate and Benazepril Hydrochloride
| NDC Code | 65862-583-05 |
| Proprietary Name | Amlodipine Besylate and Benazepril Hydrochloride |
| Package Description | 500 CAPSULE in 1 BOTTLE (65862-583-05) |
| Product NDC | 65862-583 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amlodipine Besylate and Benazepril Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120905 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Strength Number | 5; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical 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] |
