sucralfate

Generic: sucralfate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5287
Product ID 50090-5287_270e52df-d16b-4a96-b751-ff580c2f00c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018333
Listing Expiration 2026-12-31
Marketing Start 2017-09-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905287
Hyphenated Format 50090-5287

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 NDA018333 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-5287-0)
source: ndc

Packages (1)

50090-5287-0 60 TABLET in 1 BOTTLE (50090-5287-0)

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": "270e52df-d16b-4a96-b751-ff580c2f00c4", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["793d033d-d341-4910-8dda-d43d8fd03a4d"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5287-0)", "package_ndc": "50090-5287-0", "marketing_start_date": "20201022"}], "brand_name": "Sucralfate", "product_id": "50090-5287_270e52df-d16b-4a96-b751-ff580c2f00c4", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "50090-5287", "generic_name": "Sucralfate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "NDA018333", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20170925", "listing_expiration_date": "20261231"}