Sucralfate

Product NDC

55154-4057

11-digit product format

551544057

Labeler code

55154

Product ID

55154-4057_4937b200-d55c-40ac-8a7c-486458dce644

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sucralfate

Dosage form

SUSPENSION

Route

ORAL

Labeler

Cardinal Health

Application

NDA019183

Marketing category

NDA

Marketing start

2012-08-16

Marketing end

0000-00-00

Substance

SUCRALFATE

Active strength

1 g/10mL

Pharmacologic classes

Aluminum Complex [EPC],Organometallic Compounds [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record