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 68788-8779
Product ID 68788-8779_657d271c-f93e-4356-a043-e8c383b4a023
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215705
Listing Expiration 2027-12-31
Marketing Start 2024-12-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888779
Hyphenated Format 68788-8779

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 ANDA215705 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-8779-3)
  • 100 TABLET in 1 BOTTLE (68788-8779-9)
source: ndc

Packages (2)

68788-8779-3 30 TABLET in 1 BOTTLE (68788-8779-3) 68788-8779-9 100 TABLET in 1 BOTTLE (68788-8779-9)

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": "657d271c-f93e-4356-a043-e8c383b4a023", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["a434bf8f-cc60-4d84-a9a4-61c3ff6b700e"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8779-3)", "package_ndc": "68788-8779-3", "marketing_start_date": "20241210"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8779-9)", "package_ndc": "68788-8779-9", "marketing_start_date": "20241210"}], "brand_name": "Sucralfate", "product_id": "68788-8779_657d271c-f93e-4356-a043-e8c383b4a023", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68788-8779", "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": "ANDA215705", "marketing_category": "ANDA", "marketing_start_date": "20241210", "listing_expiration_date": "20271231"}