Benazepril Hydrochloride And Hydrochlorothiazide 68462-0576
Product NDC
68462-0576- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 17, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA076631
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 5 mg/1 |
| Hydrochlorothiazide | 6.25 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (68462-576-01)