Digoxin

Product NDC

70518-1250

11-digit product format

705181250

Labeler code

70518

Product ID

70518-1250_910255b4-9fb9-6089-e053-2995a90af845

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Digoxin

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077002

Marketing category

ANDA

Marketing start

2018-06-11

Marketing end

0000-00-00

Substance

DIGOXIN

Active strength

125 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