sucralfate
Generic: sucralfate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
sucralfate
Generic Name
sucralfate
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
sucralfate 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2114
Product ID
71335-2114_fc506a9a-8d99-f22b-e053-6394a90ad6d9
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
713352114
Hyphenated Format
71335-2114
Supplemental Identifiers
RxCUI
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
- 28 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0)
- 100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1)
- 60 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2)
- 30 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3)
- 20 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4)
- 150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6)
- 90 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7)
- 40 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8)
- 120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9)
Packages (9)
71335-2114-0
28 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0)
71335-2114-1
100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1)
71335-2114-2
60 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2)
71335-2114-3
30 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3)
71335-2114-4
20 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4)
71335-2114-6
150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6)
71335-2114-7
90 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7)
71335-2114-8
40 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8)
71335-2114-9
120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc506a9a-8d99-f22b-e053-6394a90ad6d9", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["370f5ac6-2c64-42ef-ab5d-075a473012f1"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0)", "package_ndc": "71335-2114-0", "marketing_start_date": "20220620"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1)", "package_ndc": "71335-2114-1", "marketing_start_date": "20220620"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2)", "package_ndc": "71335-2114-2", "marketing_start_date": "20220620"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3)", "package_ndc": "71335-2114-3", "marketing_start_date": "20220620"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4)", "package_ndc": "71335-2114-4", "marketing_start_date": "20220620"}, {"sample": false, "description": "150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6)", "package_ndc": "71335-2114-6", "marketing_start_date": "20220620"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7)", "package_ndc": "71335-2114-7", "marketing_start_date": "20220620"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8)", "package_ndc": "71335-2114-8", "marketing_start_date": "20220620"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9)", "package_ndc": "71335-2114-9", "marketing_start_date": "20220620"}], "brand_name": "Sucralfate", "product_id": "71335-2114_fc506a9a-8d99-f22b-e053-6394a90ad6d9", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "71335-2114", "generic_name": "Sucralfate", "labeler_name": "Bryant Ranch Prepack", "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"}