sucralfate

Generic: sucralfate

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3812
Product ID 68071-3812_31a7e09b-5fe1-f1fc-e063-6394a90a63d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215705
Listing Expiration 2026-12-31
Marketing Start 2023-05-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713812
Hyphenated Format 68071-3812

Supplemental Identifiers

RxCUI
314234
UPC
0368071381238
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 (68071-3812-3)
source: ndc

Packages (1)

68071-3812-3 30 TABLET in 1 BOTTLE (68071-3812-3)

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": "31a7e09b-5fe1-f1fc-e063-6394a90a63d9", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0368071381238"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["31a7dcd0-e677-249a-e063-6294a90a75f6"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3812-3)", "package_ndc": "68071-3812-3", "marketing_start_date": "20250319"}], "brand_name": "Sucralfate", "product_id": "68071-3812_31a7e09b-5fe1-f1fc-e063-6394a90a63d9", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68071-3812", "generic_name": "Sucralfate", "labeler_name": "NuCare 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": "20230520", "listing_expiration_date": "20261231"}