Moexipril Hydrochloride 00093-0017-01

Package NDC

00093-0017-01

Manufacturer: Teva Pharmaceuticals Usa, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 8, 2003
Listing Expires: December 31, 2026
Application: ANDA076204

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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

00093-0017-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)