DailyMed label

Sucralfate

DailyMed label · Kesin Pharma Corporation · version 1

Key facts

Product Sucralfate
Labeler Kesin Pharma Corporation
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients SUCRALFATE
Active ingredient UNIIs XX73205DH5
Application number 216474
Route ORAL
NDC package codes 81033-149-10, 81033-149-44, 81033-149-52
Effective date Jul 1, 2025
Set ID 36d940f2-207b-68c5-e063-6294a90a6b4a

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • 1–9 Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About DailyMed drug labels

DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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