sucralfate

Generic: sucralfate

Labeler: kesin pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler kesin pharma corporation
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Kesin Pharma Corporation

Identifiers & Regulatory

Product NDC 81033-149
Product ID 81033-149_36d940f2-207c-68c5-e063-6294a90a6b4a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216474
Listing Expiration 2026-12-31
Marketing Start 2024-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81033149
Hyphenated Format 81033-149

Supplemental Identifiers

RxCUI
313123
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 ANDA216474 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 40 CUP, UNIT-DOSE in 1 CARTON (81033-149-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)
  • 100 CUP, UNIT-DOSE in 1 CASE (81033-149-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)
source: ndc

Packages (2)

81033-149-44 40 CUP, UNIT-DOSE in 1 CARTON (81033-149-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10) 81033-149-52 100 CUP, UNIT-DOSE in 1 CASE (81033-149-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)

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": "36d940f2-207c-68c5-e063-6294a90a6b4a", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["36d940f2-207b-68c5-e063-6294a90a6b4a"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CARTON (81033-149-44)  / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)", "package_ndc": "81033-149-44", "marketing_start_date": "20240701"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-149-52)  / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)", "package_ndc": "81033-149-52", "marketing_start_date": "20240701"}], "brand_name": "Sucralfate", "product_id": "81033-149_36d940f2-207c-68c5-e063-6294a90a6b4a", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "81033-149", "generic_name": "Sucralfate", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA216474", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}