sucralfate

Generic: sucralfate

Labeler: viona pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler viona pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Viona Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 72578-081
Product ID 72578-081_a60d75d8-56a3-489e-9806-3b2f9fb6d553
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 72578081
Hyphenated Format 72578-081

Supplemental Identifiers

RxCUI
314234
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 ANDA215705 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72578-081-01)
  • 500 TABLET in 1 BOTTLE (72578-081-05)
  • 30 TABLET in 1 BOTTLE (72578-081-06)
source: ndc

Packages (3)

72578-081-01 100 TABLET in 1 BOTTLE (72578-081-01) 72578-081-05 500 TABLET in 1 BOTTLE (72578-081-05) 72578-081-06 30 TABLET in 1 BOTTLE (72578-081-06)

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": "a60d75d8-56a3-489e-9806-3b2f9fb6d553", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["c708201b-2618-4470-a3ff-8ecf04d6b3a0"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72578-081-01)", "package_ndc": "72578-081-01", "marketing_start_date": "20230520"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72578-081-05)", "package_ndc": "72578-081-05", "marketing_start_date": "20230520"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72578-081-06)", "package_ndc": "72578-081-06", "marketing_start_date": "20230520"}], "brand_name": "Sucralfate", "product_id": "72578-081_a60d75d8-56a3-489e-9806-3b2f9fb6d553", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "72578-081", "generic_name": "Sucralfate", "labeler_name": "Viona 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"}