Benazepril Hydrochloride (Rebel Distributors Corp.)


Welcome to the PulseAid listing for the Benazepril Hydrochloride drug offered from Rebel Distributors Corp.. This Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] 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: Rebel Distributors Corp.
NON-PROPRIETARY NAME: Benazepril Hydrochloride
SUBSTANCE NAME: D&C YELLOW NO. 10
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2004-02-11
END MARKETING DATE: 0000-00-00


Benazepril Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBenazepril Hydrochloride from Rebel Distributors Corp.
LABELER NAME: Rebel Distributors Corp.
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/1)
START MARKETING DATE: 2004-02-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 21695-326_56ffd662-60a6-4b43-a7ea-f778714dfbbd
PRODUCT NDC: 21695-326
APPLICATION NUMBER: ANDA076402

Other D&C YELLOW NO. 10 Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Rebel Distributors Corp.Benazepril Hydrochloride