DIGOX

Product NDC

49999-181

11-digit product format

499990181

Labeler code

49999

Product ID

49999-181_d6f680f0-4fcd-4997-afad-f2a8520093b9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Digoxin

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076268

Marketing category

ANDA

Marketing start

2002-07-26

Marketing end

0000-00-00

Substance

DIGOXIN

Active strength

250 ug/1

Pharmacologic classes

Cardiac Glycoside [EPC],Cardiac Glycosides [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record