Benazepril Hydrochloride 50090-3359
Product NDC
50090-3359- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 22, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA078212
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 40 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0)
90 TABLET, FILM COATED in 1 BOTTLE (50090-3359-1)