sucralfate

Generic: sucralfate

Labeler: pacific pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler pacific pharma, inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Pacific Pharma, Inc.

Identifiers & Regulatory

Product NDC 82182-106
Product ID 82182-106_e171ec84-fb54-4598-a9e8-e37413ef2c64
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA019183
Listing Expiration 2026-12-31
Marketing Start 2024-02-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82182106
Hyphenated Format 82182-106

Supplemental Identifiers

RxCUI
313123
UPC
0382182106146
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 (source: ndc)
Application Number NDA019183 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 420 mL in 1 BOTTLE (82182-106-14)
source: ndc

Packages (1)

82182-106-14 420 mL in 1 BOTTLE (82182-106-14)

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": "e171ec84-fb54-4598-a9e8-e37413ef2c64", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0382182106146"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["7407c58e-766f-4e93-a1bb-c77892ae0174"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Pacific Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (82182-106-14)", "package_ndc": "82182-106-14", "marketing_start_date": "20240201"}], "brand_name": "Sucralfate", "product_id": "82182-106_e171ec84-fb54-4598-a9e8-e37413ef2c64", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "82182-106", "generic_name": "Sucralfate", "labeler_name": "Pacific Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "NDA019183", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}