sucralfate

Generic: sucralfate oral suspension

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate oral suspension
Labeler major pharmaceuticals
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7470
Product ID 0904-7470_91b1db83-0f5e-4433-9104-6a2c315d13c8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211884
Listing Expiration 2027-12-31
Marketing Start 2024-06-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047470
Hyphenated Format 0904-7470

Supplemental Identifiers

RxCUI
313123
UPC
0309047470662
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 suspension (source: ndc)
Application Number ANDA211884 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 30 CUP, UNIT-DOSE in 1 CASE (0904-7470-01) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • 40 CUP, UNIT-DOSE in 1 CARTRIDGE (0904-7470-18) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • 20 CUP, UNIT-DOSE in 1 CASE (0904-7470-56) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • 100 CUP, UNIT-DOSE in 1 CASE (0904-7470-72) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • 50 CUP, UNIT-DOSE in 1 CASE (0904-7470-95) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
source: ndc

Packages (6)

0904-7470-01 30 CUP, UNIT-DOSE in 1 CASE (0904-7470-01) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) 0904-7470-18 40 CUP, UNIT-DOSE in 1 CARTRIDGE (0904-7470-18) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) 0904-7470-56 20 CUP, UNIT-DOSE in 1 CASE (0904-7470-56) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) 0904-7470-66 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) 0904-7470-72 100 CUP, UNIT-DOSE in 1 CASE (0904-7470-72) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) 0904-7470-95 50 CUP, UNIT-DOSE in 1 CASE (0904-7470-95) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)

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": "91b1db83-0f5e-4433-9104-6a2c315d13c8", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0309047470662"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["98a8fedd-fa06-416a-8a85-b899631978f9"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CUP, UNIT-DOSE in 1 CASE (0904-7470-01)  / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-01", "marketing_start_date": "20240626"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CARTRIDGE (0904-7470-18)  / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-18", "marketing_start_date": "20240626"}, {"sample": false, "description": "20 CUP, UNIT-DOSE in 1 CASE (0904-7470-56)  / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-56", "marketing_start_date": "20240626"}, {"sample": false, "description": "10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-66", "marketing_start_date": "20240626"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (0904-7470-72)  / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-72", "marketing_start_date": "20240626"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (0904-7470-95)  / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-95", "marketing_end_date": "20261031", "marketing_start_date": "20240626"}], "brand_name": "Sucralfate", "product_id": "0904-7470_91b1db83-0f5e-4433-9104-6a2c315d13c8", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "0904-7470", "generic_name": "SUCRALFATE Oral Suspension", "labeler_name": "Major Pharmaceuticals", "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": "20240626", "listing_expiration_date": "20271231"}