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
63629-9152
Product ID
63629-9152_68eb54fd-5a5e-4803-a43e-1c3134416377
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
636299152
Hyphenated Format
63629-9152
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
- 100 TABLET in 1 BOTTLE, PLASTIC (63629-9152-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "68eb54fd-5a5e-4803-a43e-1c3134416377", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["7b05323d-4695-41d7-8236-1e7b4e8f2a1e"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-9152-1)", "package_ndc": "63629-9152-1", "marketing_start_date": "20220126"}], "brand_name": "Sucralfate", "product_id": "63629-9152_68eb54fd-5a5e-4803-a43e-1c3134416377", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "63629-9152", "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"}