Moexipril Hydrochloride 62135-0969

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

Ingredient	Strength
Moexipril Hydrochloride	15 mg/1

Drug Class

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

Packaging Options(1)

62135-0969-90

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

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