sucralfate

Generic: sucralfate oral

Labeler: trupharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate oral
Labeler trupharma, llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
TruPharma, LLC

Identifiers & Regulatory

Product NDC 52817-840
Product ID 52817-840_4718799e-e742-c93e-e063-6294a90aacfd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213549
Listing Expiration 2026-12-31
Marketing Start 2024-04-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52817840
Hyphenated Format 52817-840

Supplemental Identifiers

RxCUI
313123
UPC
0352817840165
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 ANDA213549 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (52817-840-16)
source: ndc

Packages (1)

52817-840-16 473 mL in 1 BOTTLE (52817-840-16)

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": "4718799e-e742-c93e-e063-6294a90aacfd", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0352817840165"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["7d441128-45d2-4bf2-817b-665784992e90"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["TruPharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (52817-840-16)", "package_ndc": "52817-840-16", "marketing_start_date": "20240401"}], "brand_name": "Sucralfate", "product_id": "52817-840_4718799e-e742-c93e-e063-6294a90aacfd", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "52817-840", "generic_name": "Sucralfate Oral", "labeler_name": "TruPharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA213549", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}