Quinapril

Product NDC
62756-313
11-digit product format
627560313
Labeler code
62756
Product ID
62756-313_461bf92c-0ad0-4e99-8542-6dc6bfbde5f1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Quinapril
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sun Pharmaceutical Industries Limited
Application
ANDA090800
Marketing category
ANDA
Marketing start
2009-06-18
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
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62756-313QUINAPRIL TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES LIMITED]6Legacy NDC20101227_976577fd-f9dc-4c41-8051-9dd7f949fc87.zip