sucralfate

Generic: sucralfate oral

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate oral
Labeler avpak
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-745
Product ID 50268-745_4510a8c1-2007-1ac1-e063-6294a90a1375
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209356
Listing Expiration 2026-12-31
Marketing Start 2022-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268745
Hyphenated Format 50268-745

Supplemental Identifiers

RxCUI
313123
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 oral (source: ndc)
Application Number ANDA209356 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 40 CUP in 1 BOX (50268-745-14) / 10 mL in 1 CUP (50268-745-11)
source: ndc

Packages (1)

50268-745-14 40 CUP in 1 BOX (50268-745-14) / 10 mL in 1 CUP (50268-745-11)

Ingredients (1)

sucralfate (1 g/10mL)

Linked Drug Pages (1)

Sucralfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4510a8c1-2007-1ac1-e063-6294a90a1375", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["e78ef7d4-faa7-aebf-e053-2995a90a6f84"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 CUP in 1 BOX (50268-745-14)  / 10 mL in 1 CUP (50268-745-11)", "package_ndc": "50268-745-14", "marketing_start_date": "20220831"}], "brand_name": "Sucralfate", "product_id": "50268-745_4510a8c1-2007-1ac1-e063-6294a90a1375", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "50268-745", "generic_name": "Sucralfate Oral", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA209356", "marketing_category": "ANDA", "marketing_start_date": "20220831", "listing_expiration_date": "20261231"}