Quinapril

Product NDC

50090-2643

11-digit product format

500902643

Labeler code

50090

Product ID

50090-2643_8a640b3e-8c88-49a8-9ab4-a77ba336abd2

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

10 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