FDA.reportPublic FDA data

Quinapril

Product NDC
50090-2117
11-digit product format
500902117
Labeler code
50090
Product ID
50090-2117_3ef96276-71be-41e9-80fc-02332276b191
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Quinapril Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202725
Marketing category
ANDA
Marketing start
2013-04-29
Marketing end
0000-00-00
Substance
QUINAPRIL HYDROCHLORIDE
Active strength
40 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9992a562-005f-c280-535c-2e4eaa81efcdProduct name220161121
59212689-39e5-a976-6d21-882d76d8079aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-2117-02023-01-30C16284748780-1f386c649-a20f-0266-e053-dadaa90a7c1aQuinapril Tablets, USP Rx only
50090-2117-12023-01-30C16284748780-1f386c649-a20f-0266-e053-dadaa90a7c1aQuinapril Tablets, USP Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-2117-0Quinapril30 in 1 BOTTLETABLET, FILM COATED3021
50090-2117-1Quinapril90 in 1 BOTTLETABLET, FILM COATED9021

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2117-0EA - Each50090-2117288837e5-dc7d-4522-b461-6838fa13cff312019-02-13
50090-2117-1EA - Each50090-21175c301e94-f21f-40c7-b49a-25ac95f5b24c12019-02-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-2117QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]21Legacy NDC, 2 package rows20210818_913c359f-160c-4cd9-88f7-ae1c74340e49.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312749quinapril HCl 20 MG Oral TabletPSN913c359f-160c-4cd9-88f7-ae1c74340e4921
314203quinapril HCl 40 MG Oral TabletPSN913c359f-160c-4cd9-88f7-ae1c74340e4921
312749quinapril 20 MG Oral TabletSCD913c359f-160c-4cd9-88f7-ae1c74340e4921
314203quinapril 40 MG Oral TabletSCD913c359f-160c-4cd9-88f7-ae1c74340e4921
312749quinapril (as quinapril HCl) 20 MG Oral TabletSY913c359f-160c-4cd9-88f7-ae1c74340e4921
314203quinapril (as quinapril hydrochloride) 40 MG Oral TabletSY913c359f-160c-4cd9-88f7-ae1c74340e4921

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-2117-05009021170030 TABLET, FILM COATED in 1 BOTTLE (50090-2117-0) 2015-10-140000-00-00NoNoCurrent
50090-2117-15009021170190 TABLET, FILM COATED in 1 BOTTLE (50090-2117-1) 2017-07-310000-00-00NoNoCurrent