NDCFind

Benazepril Hydrochloride 82868-0089-30

Package NDC

82868-0089-30

Product NDC: 82868-0089

Manufacturer
Northwind Health Company, Llc
Dosage Form
Tablet, Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
October 2, 2025
Listing Expires
December 31, 2026
Application
ANDA076118
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Active Ingredients

IngredientStrength
Benazepril Hydrochloride40 mg/1

Drug Class

Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]

Selected Package

82868-0089-30Selected

30 TABLET, COATED in 1 BOTTLE, PLASTIC (82868-089-30)