Moexipril Hydrochloride 62135-0967-90

Package NDC

62135-0967-90

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

Ingredient	Strength
Moexipril Hydrochloride	7.5 mg/1

Drug Class

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

Selected Package

62135-0967-90Selected

90 TABLET, FILM COATED in 1 BOTTLE (62135-967-90)