sucralfate

Generic: sucralfate

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-1656
Product ID 69238-1656_507ba68d-7593-4545-bbe1-dc9463c1a893
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215576
Listing Expiration 2026-12-31
Marketing Start 2022-04-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692381656
Hyphenated Format 69238-1656

Supplemental Identifiers

RxCUI
314234
UPC
0369238165616
UNII
XX73205DH5
NUI
N0000175801 M0015420

Packaging Origin

Original Packager
true

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 ANDA215576 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69238-1656-1)
  • 500 TABLET in 1 BOTTLE (69238-1656-5)
source: ndc

Packages (2)

69238-1656-1 100 TABLET in 1 BOTTLE (69238-1656-1) 69238-1656-5 500 TABLET in 1 BOTTLE (69238-1656-5)

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": "507ba68d-7593-4545-bbe1-dc9463c1a893", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0369238165616"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["a4f722e7-2885-4f27-8358-9c662439600a"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-1656-1)", "package_ndc": "69238-1656-1", "marketing_start_date": "20220422"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69238-1656-5)", "package_ndc": "69238-1656-5", "marketing_start_date": "20220523"}], "brand_name": "Sucralfate", "product_id": "69238-1656_507ba68d-7593-4545-bbe1-dc9463c1a893", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "69238-1656", "generic_name": "Sucralfate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA215576", "marketing_category": "ANDA", "marketing_start_date": "20220422", "listing_expiration_date": "20261231"}