DIGOXIN

Product NDC

49884-494

11-digit product format

498840494

Labeler code

49884

Product ID

49884-494_86c8d078-9090-4b77-adc6-49abfcdd74dd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DIGOXIN

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical Inc.

Application

NDA020405

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-01-14

Marketing end

2020-08-31

Substance

DIGOXIN

Active strength

0 mg/1

Pharmacologic classes

Cardiac Glycoside [EPC],Cardiac Glycosides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record