FDA.reportPublic FDA data

Quinapril

Product NDC
68071-3258
11-digit product format
680713258
Labeler code
68071
Product ID
68071-3258_4f43ca14-d456-0a66-e054-00144ff8d46c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Quinapril Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA202725
Marketing category
ANDA
Marketing start
2013-04-29
Marketing end
0000-00-00
Substance
QUINAPRIL HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-3258-32020-05-08C16284748780-19d75b9cf-d2d7-f424-e053-dadaa90a57ce4f43ca14-d455-0a66-e054-00144ff8d46c
68071-3258-82020-05-08C16284748780-19d75b9cf-d2d7-f424-e053-dadaa90a57ce4f43ca14-d455-0a66-e054-00144ff8d46c
68071-3258-32020-01-31C16284748780-19d75b9cf-d2d7-f424-e053-dadaa90a57ce4f43ca14-d455-0a66-e054-00144ff8d46c
68071-3258-82020-01-31C16284748780-19d75b9cf-d2d7-f424-e053-dadaa90a57ce4f43ca14-d455-0a66-e054-00144ff8d46c