sucralfate

Generic: sucralfate

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler atlantic biologicals corp.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0306
Product ID 17856-0306_361f83ba-0caa-c1c1-e063-6394a90a4c10
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 178560306
Hyphenated Format 17856-0306

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
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1) / 10 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (1)

17856-0306-1 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1) / 10 mL in 1 CUP, UNIT-DOSE

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": "361f83ba-0caa-c1c1-e063-6394a90a4c10", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["e5073597-ac51-4e7c-a9dc-7695773a01f1"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1)  / 10 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-0306-1", "marketing_start_date": "20230810"}], "brand_name": "Sucralfate", "product_id": "17856-0306_361f83ba-0caa-c1c1-e063-6394a90a4c10", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "17856-0306", "generic_name": "Sucralfate", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "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"}