sucralfate

Generic: sucralfate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler american health packaging
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-738
Product ID 60687-738_02935a29-75bc-0f18-e063-6294a90a1405
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211884
Listing Expiration 2026-12-31
Marketing Start 2023-08-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687738
Hyphenated Format 60687-738

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 ANDA211884 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 3 TRAY in 1 CASE (60687-738-08) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)
  • 4 TRAY in 1 CASE (60687-738-23) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)
  • 10 TRAY in 1 CASE (60687-738-56) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)
source: ndc

Packages (3)

Ingredients (1)

sucralfate (1 g/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "02935a29-75bc-0f18-e063-6294a90a1405", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["e4761fb2-6a1a-44de-9d27-f6addabc24c8"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (60687-738-08)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48)  / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)", "package_ndc": "60687-738-08", "marketing_start_date": "20230801"}, {"sample": false, "description": "4 TRAY in 1 CASE (60687-738-23)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48)  / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)", "package_ndc": "60687-738-23", "marketing_start_date": "20230801"}, {"sample": false, "description": "10 TRAY in 1 CASE (60687-738-56)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48)  / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)", "package_ndc": "60687-738-56", "marketing_start_date": "20230801"}], "brand_name": "Sucralfate", "product_id": "60687-738_02935a29-75bc-0f18-e063-6294a90a1405", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "60687-738", "generic_name": "Sucralfate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA211884", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}