sucralfate

Generic: sucralfate oral

Labeler: precision dose, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate oral
Labeler precision dose, inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Precision Dose, Inc.

Identifiers & Regulatory

Product NDC 68094-041
Product ID 68094-041_f2fb0919-1f13-4ca2-bf04-254c1e44b86c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209356
Listing Expiration 2026-12-31
Marketing Start 2025-01-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68094041
Hyphenated Format 68094-041

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 oral (source: ndc)
Application Number ANDA209356 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 10 TRAY in 1 CASE (68094-041-61) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)
  • 3 TRAY in 1 CASE (68094-041-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)
source: ndc

Packages (2)

68094-041-61 10 TRAY in 1 CASE (68094-041-61) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59) 68094-041-62 3 TRAY in 1 CASE (68094-041-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)

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": "f2fb0919-1f13-4ca2-bf04-254c1e44b86c", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["0dc592e9-541c-4fac-8ab5-829d43521c01"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Precision Dose, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (68094-041-61)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)", "package_ndc": "68094-041-61", "marketing_start_date": "20250130"}, {"sample": false, "description": "3 TRAY in 1 CASE (68094-041-62)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)", "package_ndc": "68094-041-62", "marketing_start_date": "20250130"}], "brand_name": "Sucralfate", "product_id": "68094-041_f2fb0919-1f13-4ca2-bf04-254c1e44b86c", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68094-041", "generic_name": "Sucralfate oral", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA209356", "marketing_category": "ANDA", "marketing_start_date": "20250130", "listing_expiration_date": "20261231"}