sucralfate

Generic: sucralfate

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

Drug Facts

Product Profile

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

sucralfate 1 g/10mL

Manufacturer
VistaPharm, LLC

Identifiers & Regulatory

Product NDC 66689-305
Product ID 66689-305_f133ac10-0969-47cb-932a-7b100b05105c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211884
Listing Expiration 2026-12-31
Marketing Start 2022-03-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66689305
Hyphenated Format 66689-305

Supplemental Identifiers

RxCUI
313123
UPC
0366689305165
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 ANDA211884 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (66689-305-16) / 414 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

66689-305-16 1 BOTTLE, PLASTIC in 1 CARTON (66689-305-16) / 414 mL in 1 BOTTLE, PLASTIC

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": "f133ac10-0969-47cb-932a-7b100b05105c", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0366689305165"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["cbfbe146-5d42-4a55-9050-df2b5581487a"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (66689-305-16)  / 414 mL in 1 BOTTLE, PLASTIC", "package_ndc": "66689-305-16", "marketing_start_date": "20220315"}], "brand_name": "Sucralfate", "product_id": "66689-305_f133ac10-0969-47cb-932a-7b100b05105c", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "66689-305", "generic_name": "Sucralfate", "labeler_name": "VistaPharm, LLC", "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": "20220315", "listing_expiration_date": "20261231"}