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Benazepril Hydrochloride
Benazepril Hydrochloride - 65862-117-01 - (Benazepril Hydrochloride)
Drug Information of Benazepril Hydrochloride
| Product NDC: | 65862-117 |
| Proprietary Name: | Benazepril Hydrochloride |
| Non Proprietary Name: | Benazepril Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Benazepril Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benazepril Hydrochloride
| Product NDC: | 65862-117 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078212 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080522 |
Package Information of Benazepril Hydrochloride
| Package NDC: | 65862-117-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01) |
NDC Information of Benazepril Hydrochloride
| NDC Code | 65862-117-01 |
| Proprietary Name | Benazepril Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01) |
| Product NDC | 65862-117 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benazepril Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080522 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | BENAZEPRIL HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
