Sucralfate

Product NDC
63629-9152
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sucralfate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA074415
Marketing category
ANDA
Substance
SUCRALFATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-9152-1100 TABLET in 1 BOTTLE, PLASTIC (63629-9152-1) 2022-01-26NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sucralfate Tablets, USP 1 gramBryant Ranch Prepack2024-01-11HUMAN PRESCRIPTION DRUG LABEL102