Moexipril Hydrochloride and Hydrochlorothiazide (AvKARE, Inc.)


Welcome to the PulseAid listing for the Moexipril Hydrochloride and Hydrochlorothiazide drug offered from AvKARE, Inc.. This Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: AvKARE, Inc.
NON-PROPRIETARY NAME: Moexipril Hydrochloride and Hydrochlorothiazide
SUBSTANCE NAME: MOEXIPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2017-04-03
END MARKETING DATE: 0000-00-00


Moexipril Hydrochloride and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMoexipril Hydrochloride and Hydrochlorothiazide from AvKARE, Inc.
LABELER NAME: AvKARE, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 7.5; 12.5(mg/1; mg/1)
START MARKETING DATE: 2017-04-03
END MARKETING DATE: 0000-00-00
PRODUCT ID: 42291-576_e7ea7d06-70bc-46fc-b7bc-5e3d49bfa181
PRODUCT NDC: 42291-576
APPLICATION NUMBER: ANDA076980

Other MOEXIPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
AvKARE, Inc.Moexipril Hydrochloride and Hydrochlorothiazide
Glenmark Pharmaceuticals Inc., USAMoexipril Hydrochloride and Hydrochlorothiazide
Heritage Pharmaceuticals Inc.Moexipril hydrochloride and hydrochlorothiazide
Teva Pharmaceuticals USA, Inc.Moexipril Hydrochloride and Hydrochlorothiazide