Quinapril Hydrochloride
Quinapril Hydrochloride Tablets
Approved
Approval ID
08ed2c17-cd53-4ad9-8b01-185d9c0ab65f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 13, 2014
Manufacturers
FDA
Carilion Materials Management
DUNS: 079239644
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
quinapril hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68151-1020
Application NumberNDA019885
Product Classification
M
Marketing Category
C73605
G
Generic Name
quinapril hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateJune 13, 2014
FDA Product Classification
INGREDIENTS (9)
QUINAPRILActive
Quantity: 5 mg in 1 1
Code: RJ84Y44811
Classification: ACTIB
CANDELILLA WAXInactive
Code: WL0328HX19
Classification: IACT
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
LACTOSEInactive
Code: J2B2A4N98G
Classification: IACT
GELATINInactive
Code: 2G86QN327L
Classification: IACT
MAGNESIUM CARBONATEInactive
Code: 0E53J927NA
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
FERRIC OXIDE REDInactive
Code: 1K09F3G675
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT