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Amlodipine Besylate and Benazepril HCL
Amlodipine Besylate and Benazepril HCL - 68084-351-21 - (Amlodipine Besylate and Benazepril HCL)
Drug Information of Amlodipine Besylate and Benazepril HCL
| Product NDC: | 68084-351 |
| Proprietary Name: | Amlodipine Besylate and Benazepril HCL |
| Non Proprietary Name: | Amlodipine Besylate and Benazepril HCL |
| Active Ingredient(s): | 10; 20 mg/1; mg/1 & nbsp; Amlodipine Besylate and Benazepril HCL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amlodipine Besylate and Benazepril HCL
| Product NDC: | 68084-351 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078466 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100922 |
Package Information of Amlodipine Besylate and Benazepril HCL
| Package NDC: | 68084-351-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-351-21) > 10 CAPSULE in 1 BLISTER PACK (68084-351-11) |
NDC Information of Amlodipine Besylate and Benazepril HCL
| NDC Code | 68084-351-21 |
| Proprietary Name | Amlodipine Besylate and Benazepril HCL |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-351-21) > 10 CAPSULE in 1 BLISTER PACK (68084-351-11) |
| Product NDC | 68084-351 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amlodipine Besylate and Benazepril HCL |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100922 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Strength Number | 10; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | 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] |
