Benazepril Hydrochloride and Hydrochlorothiazide - Benazepril Hydrochloride and Hydrochlorothiazide
Navigation: NDC > Supplier starting with: P > PHYSICIANS TOTAL CARE, INC.| Field | Value |
|---|---|
| NDC Code: | 54868-3906 |
| Proprietary Name: | Benazepril Hydrochloride and Hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | Benazepril Hydrochloride and Hydrochlorothiazide |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 28-10-2004 |
| Category Name: | ANDA |
| Application Number: | ANDA076631 |
| Labeler: | PHYSICIANS TOTAL CARE, INC. |
| Substance Name: | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: | 20; 12.5 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |