Sucralfate

Product NDC
71335-2461
11-digit product format
713352461
Labeler code
71335
Product ID
71335-2461_f0c7181f-355f-4a4a-80c4-700eab56b77d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sucralfate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA215705
Marketing category
ANDA
Marketing start
2023-05-20
Substance
SUCRALFATE
Active strength
1 g/1
Pharmacologic classes
Aluminum Complex [EPC], Organometallic Compounds [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sucralfate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SUCRALFATE1 g/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiXX73205DH5
Rxcui314234

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2461-07133524610028 TABLET in 1 BOTTLE (71335-2461-0) 28 tablet2024-08-22NoNoHistorical
71335-2461-171335246101100 TABLET in 1 BOTTLE (71335-2461-1) 100 tablet2024-08-22NoNoHistorical
71335-2461-27133524610260 TABLET in 1 BOTTLE (71335-2461-2) 60 tablet2024-08-22NoNoHistorical
71335-2461-37133524610330 TABLET in 1 BOTTLE (71335-2461-3) 30 tablet2024-08-22NoNoHistorical
71335-2461-47133524610420 TABLET in 1 BOTTLE (71335-2461-4) 20 tablet2024-08-22NoNoHistorical
71335-2461-671335246106150 TABLET in 1 BOTTLE (71335-2461-6) 150 tablet2024-08-22NoNoHistorical
71335-2461-77133524610790 TABLET in 1 BOTTLE (71335-2461-7) 90 tablet2024-08-22NoNoHistorical
71335-2461-87133524610840 TABLET in 1 BOTTLE (71335-2461-8) 40 tablet2024-08-22NoNoHistorical
71335-2461-971335246109120 TABLET in 1 BOTTLE (71335-2461-9) 120 tablet2024-08-22NoNoHistorical