sucralfate

Generic: sucralfate

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-4517
Product ID 0615-4517_7226b7de-1569-4e22-9ed3-1de5487e68ed
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 06154517
Hyphenated Format 0615-4517

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
  • 30 TABLET in 1 BLISTER PACK (0615-4517-39)
source: ndc

Packages (1)

0615-4517-39 30 TABLET in 1 BLISTER PACK (0615-4517-39)

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": "7226b7de-1569-4e22-9ed3-1de5487e68ed", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["d67dcaad-56c1-4e77-a0c8-655970808414"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-4517-39)", "package_ndc": "0615-4517-39", "marketing_start_date": "20100108"}], "brand_name": "Sucralfate", "product_id": "0615-4517_7226b7de-1569-4e22-9ed3-1de5487e68ed", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "0615-4517", "generic_name": "Sucralfate", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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"}