NDCFind

Moexipril Hydrochloride 68462-0208-01

Package NDC

68462-0208-01

Product NDC: 68462-0208

Manufacturer
Glenmark Pharmaceuticals Inc., Usa
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
December 31, 2010
Listing Expires
December 31, 2027
Application
ANDA090416
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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

68462-0208-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (68462-208-01)

Other packages for this product(2)

1000 TABLET, FILM COATED in 1 BOTTLE (68462-208-10)

90 TABLET, FILM COATED in 1 BOTTLE (68462-208-90)