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Amlodipine besylate and benazepril hydrochloride
Amlodipine besylate and benazepril hydrochloride - 49884-931-01 - (amlodipine besylate and benazepril hydrochloride)
Drug Information of Amlodipine besylate and benazepril hydrochloride
| Product NDC: | 49884-931 |
| Proprietary Name: | Amlodipine besylate and benazepril hydrochloride |
| Non Proprietary Name: | amlodipine besylate and benazepril hydrochloride |
| Active Ingredient(s): | 5; 20 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: | 49884-931 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078381 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110103 |
Package Information of Amlodipine besylate and benazepril hydrochloride
| Package NDC: | 49884-931-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (49884-931-01) |
NDC Information of Amlodipine besylate and benazepril hydrochloride
| NDC Code | 49884-931-01 |
| Proprietary Name | Amlodipine besylate and benazepril hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (49884-931-01) |
| Product NDC | 49884-931 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amlodipine besylate and benazepril hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110103 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Strength Number | 5; 20 |
| 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] |
