Sucralfate

Product NDC

55289-292

11-digit product format

552890292

Labeler code

55289

Product ID

55289-292_85c90fb3-c21e-85cc-e053-2a91aa0a6700

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sucralfate

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

NDA018333

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

1996-11-01

Marketing end

2020-03-31

Substance

SUCRALFATE

Active strength

1 g/1

Pharmacologic classes

Aluminum Complex [EPC],Organometallic Compounds [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record