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Benazepril Hydrochloride and Hydrochlorothiazide
Benazepril Hydrochloride and Hydrochlorothiazide - 58118-4745-3 - (benazepril hydrochloride and hydrochlorothiazide)
Drug Information of Benazepril Hydrochloride and Hydrochlorothiazide
| Product NDC: | 58118-4745 |
| Proprietary Name: | Benazepril Hydrochloride and Hydrochlorothiazide |
| Non Proprietary Name: | benazepril hydrochloride and hydrochlorothiazide |
| Active Ingredient(s): | 20; 12.5 mg/1; mg/1 & nbsp; benazepril hydrochloride and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benazepril Hydrochloride and Hydrochlorothiazide
| Product NDC: | 58118-4745 |
| Labeler Name: | Clinical Solutions Wholesale |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076688 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121203 |
Package Information of Benazepril Hydrochloride and Hydrochlorothiazide
| Package NDC: | 58118-4745-3 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-4745-3) |
NDC Information of Benazepril Hydrochloride and Hydrochlorothiazide
| NDC Code | 58118-4745-3 |
| Proprietary Name | Benazepril Hydrochloride and Hydrochlorothiazide |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-4745-3) |
| Product NDC | 58118-4745 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benazepril hydrochloride and hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121203 |
| Marketing Category Name | ANDA |
| Labeler Name | Clinical Solutions Wholesale |
| Substance Name | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Strength Number | 20; 12.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
