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Benazepril Hydrochloride and Hydrochlorothiazide
Benazepril Hydrochloride and Hydrochlorothiazide - 0185-0124-01 - (Benazepril Hydrochloride and Hydrochlorothiazide)
Drug Information of Benazepril Hydrochloride and Hydrochlorothiazide
| Product NDC: | 0185-0124 |
| Proprietary Name: | Benazepril Hydrochloride and Hydrochlorothiazide |
| Non Proprietary Name: | Benazepril Hydrochloride and Hydrochlorothiazide |
| Active Ingredient(s): | 5; 6.25 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: | 0185-0124 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076631 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040211 |
Package Information of Benazepril Hydrochloride and Hydrochlorothiazide
| Package NDC: | 0185-0124-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0185-0124-01) |
NDC Information of Benazepril Hydrochloride and Hydrochlorothiazide
| NDC Code | 0185-0124-01 |
| Proprietary Name | Benazepril Hydrochloride and Hydrochlorothiazide |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0185-0124-01) |
| Product NDC | 0185-0124 |
| 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 | 20040211 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Strength Number | 5; 6.25 |
| 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] |
