sucralfate

Generic: sucralfate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sucralfate 1 g/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-063
Product ID 82804-063_a42c5f3d-85f1-485b-91e6-58c25b3ddc71
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070848
Listing Expiration 2026-12-31
Marketing Start 1996-11-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804063
Hyphenated Format 82804-063

Supplemental Identifiers

RxCUI
314234
UPC
0382804063307
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
  • 30 TABLET in 1 BOTTLE (82804-063-30)
  • 60 TABLET in 1 BOTTLE (82804-063-60)
  • 90 TABLET in 1 BOTTLE (82804-063-90)
source: ndc

Packages (3)

82804-063-30 30 TABLET in 1 BOTTLE (82804-063-30) 82804-063-60 60 TABLET in 1 BOTTLE (82804-063-60) 82804-063-90 90 TABLET in 1 BOTTLE (82804-063-90)

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": "a42c5f3d-85f1-485b-91e6-58c25b3ddc71", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0382804063307"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["a42c5f3d-85f1-485b-91e6-58c25b3ddc71"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-063-30)", "package_ndc": "82804-063-30", "marketing_start_date": "20240130"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-063-60)", "package_ndc": "82804-063-60", "marketing_start_date": "20240130"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-063-90)", "package_ndc": "82804-063-90", "marketing_start_date": "20240130"}], "brand_name": "Sucralfate", "product_id": "82804-063_a42c5f3d-85f1-485b-91e6-58c25b3ddc71", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "82804-063", "generic_name": "Sucralfate", "labeler_name": "Proficient Rx LP", "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": "19961111", "listing_expiration_date": "20261231"}