Strength
7.5 mg/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00093001701
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
MOEXIPRIL HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA076204On Market Since
5/8/2003
Pharmacological Classes
Angiotensin Converting Enzyme Inhibitor
Angiotensin-converting Enzyme Inhibitors
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