sucralfate

Generic: sucralfate

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-234
Product ID 72189-234_2c285743-2fa6-4132-e063-6294a90adaff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070848
Listing Expiration 2026-12-31
Marketing Start 2021-06-18

Pharmacologic Class

Established (EPC)
aluminum complex [epc]
Chemical Structure
organometallic compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189234
Hyphenated Format 72189-234

Supplemental Identifiers

RxCUI
314234
UNII
XX73205DH5
NUI
N0000175801 M0015420

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sucralfate (source: ndc)
Generic Name sucralfate (source: ndc)
Application Number ANDA070848 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (72189-234-20)
  • 90 TABLET in 1 BOTTLE (72189-234-90)
source: ndc

Packages (2)

72189-234-20 20 TABLET in 1 BOTTLE (72189-234-20) 72189-234-90 90 TABLET in 1 BOTTLE (72189-234-90)

Ingredients (1)

sucralfate (1 g/1)

Linked Drug Pages (1)

SUCRALFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c285743-2fa6-4132-e063-6294a90adaff", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["c50b5044-31ed-672a-e053-2995a90a49fc"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-234-20)", "package_ndc": "72189-234-20", "marketing_start_date": "20210618"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-234-90)", "package_ndc": "72189-234-90", "marketing_start_date": "20210618"}], "brand_name": "SUCRALFATE", "product_id": "72189-234_2c285743-2fa6-4132-e063-6294a90adaff", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "72189-234", "generic_name": "SUCRALFATE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUCRALFATE", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA070848", "marketing_category": "ANDA", "marketing_start_date": "20210618", "listing_expiration_date": "20261231"}