sucralfate
Generic: sucralfate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
sucralfate
Generic Name
sucralfate
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
sucralfate 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-102
Product ID
82804-102_51459cdb-a04a-49c2-8ee4-8f234f522476
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074415
Listing Expiration
2026-12-31
Marketing Start
2020-02-17
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804102
Hyphenated Format
82804-102
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA074415 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (82804-102-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "51459cdb-a04a-49c2-8ee4-8f234f522476", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0382804102303"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["51459cdb-a04a-49c2-8ee4-8f234f522476"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82804-102-30)", "package_ndc": "82804-102-30", "marketing_start_date": "20240506"}], "brand_name": "Sucralfate", "product_id": "82804-102_51459cdb-a04a-49c2-8ee4-8f234f522476", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "82804-102", "generic_name": "Sucralfate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA074415", "marketing_category": "ANDA", "marketing_start_date": "20200217", "listing_expiration_date": "20261231"}