sucralfate

Generic: sucralfate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8946
Product ID 68788-8946_6a99f537-9850-4eb9-8fbe-988cfcc728be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070848
Listing Expiration 2026-12-31
Marketing Start 2015-10-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888946
Hyphenated Format 68788-8946

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
  • 100 TABLET in 1 BOTTLE (68788-8946-1)
  • 30 TABLET in 1 BOTTLE (68788-8946-3)
source: ndc

Packages (2)

68788-8946-1 100 TABLET in 1 BOTTLE (68788-8946-1) 68788-8946-3 30 TABLET in 1 BOTTLE (68788-8946-3)

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": "6a99f537-9850-4eb9-8fbe-988cfcc728be", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["5ec71444-cc55-47bd-8abc-b3cfc3b47d8e"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8946-1)", "package_ndc": "68788-8946-1", "marketing_start_date": "20151028"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8946-3)", "package_ndc": "68788-8946-3", "marketing_start_date": "20151028"}], "brand_name": "Sucralfate", "product_id": "68788-8946_6a99f537-9850-4eb9-8fbe-988cfcc728be", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68788-8946", "generic_name": "Sucralfate", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20151027", "listing_expiration_date": "20261231"}