sucralfate

Generic: sucralfate

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-541
Product ID 71610-541_2f340031-6d65-4f5d-8a70-cd247c832a81
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074415
Listing Expiration 2026-12-31
Marketing Start 2020-02-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610541
Hyphenated Format 71610-541

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 ANDA074415 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (71610-541-60)
  • 120 TABLET in 1 BOTTLE, PLASTIC (71610-541-70)
  • 360 TABLET in 1 BOTTLE, PLASTIC (71610-541-94)
source: ndc

Packages (3)

Ingredients (1)

sucralfate (1 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2f340031-6d65-4f5d-8a70-cd247c832a81", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["b414dc07-681c-4fde-965f-09df64c015e7"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71610-541-60)", "package_ndc": "71610-541-60", "marketing_start_date": "20210413"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (71610-541-70)", "package_ndc": "71610-541-70", "marketing_start_date": "20210413"}, {"sample": false, "description": "360 TABLET in 1 BOTTLE, PLASTIC (71610-541-94)", "package_ndc": "71610-541-94", "marketing_start_date": "20210413"}], "brand_name": "Sucralfate", "product_id": "71610-541_2f340031-6d65-4f5d-8a70-cd247c832a81", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "71610-541", "generic_name": "Sucralfate", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA074415", "marketing_category": "ANDA", "marketing_start_date": "20200217", "listing_expiration_date": "20261231"}