Quinapril Hydrochloride

Product NDC: 68151-1022
11-digit product format: 681511022
Labeler code: 68151
Product ID: 68151-1022_0e0c7ebe-bdf1-4e38-8ab0-7c25b1dbd032
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: quinapril hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Carilion Materials Management
Application: NDA019885
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 1991-11-19
Marketing end: 0000-00-00
Substance: QUINAPRIL
Active strength: 20 mg/1
Pharmacologic classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9992a562-005f-c280-535c-2e4eaa81efcd	Product name	2	20161121
59212689-39e5-a976-6d21-882d76d8079a	Product name	1	20140508

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68151-1022-1	2020-01-31	C162847	48780-1	9d75b9d0-caea-f424-e053-dadaa90a57ce	Quinapril Hydrochloride Tablets

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68151-1022-1	Quinapril Hydrochloride	1 in 1 PACKAGE	TABLET, FILM COATED	1		2

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
QUINAPRIL	ACTIVE INGREDIENT	RJ84Y44811	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
QUINAPRILAT	ACTIVE MOIETY	34SSX5LDE5	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
CANDELILLA WAX	INACTIVE INGREDIENT	WL0328HX19	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
GELATIN	INACTIVE INGREDIENT	2G86QN327L	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
MAGNESIUM CARBONATE	INACTIVE INGREDIENT	0E53J927NA	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68151-1022	QUINAPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]	2	Legacy NDC, 1 package rows	20140718_4d009c66-2b61-43e1-8378-a9c06e972f7f.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
RJ84Y44811	QUINAPRIL	85441-61-8	QUINAPRIL
33067B3N2M	QUINAPRIL HYDROCHLORIDE	82586-55-8	quinapril hydrochloride

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312749	quinapril HCl 20 MG Oral Tablet	PSN	4d009c66-2b61-43e1-8378-a9c06e972f7f	2
312749	quinapril 20 MG Oral Tablet	SCD	4d009c66-2b61-43e1-8378-a9c06e972f7f	2
312749	quinapril (as quinapril HCl) 20 MG Oral Tablet	SY	4d009c66-2b61-43e1-8378-a9c06e972f7f	2

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
68151-1022-1	68151102201	1 in 1 PACKAGE	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Quinapril Hydrochloride Tablets	Carilion Materials Management	2014-06-13	HUMAN PRESCRIPTION DRUG LABEL	2