NDCFind

Moexipril Hydrochloride 62135-0969-90

Package NDC

62135-0969-90

Product NDC: 62135-0969

Manufacturer
Chartwell Rx, Llc
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 30, 2006
Listing Expires
December 31, 2026
Application
ANDA077536
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Active Ingredients

IngredientStrength
Moexipril Hydrochloride15 mg/1

Drug Class

Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]

Selected Package

62135-0969-90Selected

90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90)