sucralfate

Generic: sucralfate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-695
Product ID 60687-695_37dbc9fb-25b5-30a2-e063-6294a90a78b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074415
Marketing Start 2023-05-11
Marketing End 2026-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687695
Hyphenated Format 60687-695

Supplemental Identifiers

RxCUI
314234
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 (source: ndc)
Application Number ANDA074415 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-695-01) / 1 TABLET in 1 BLISTER PACK (60687-695-11)
source: ndc

Packages (1)

60687-695-01 100 BLISTER PACK in 1 CARTON (60687-695-01) / 1 TABLET in 1 BLISTER PACK (60687-695-11)

Ingredients (1)

sucralfate (1 g/1)

Linked Drug Pages (1)

Sucralfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37dbc9fb-25b5-30a2-e063-6294a90a78b8", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["e7364686-3638-4061-ae4a-62b1df7af9d0"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-695-01)  / 1 TABLET in 1 BLISTER PACK (60687-695-11)", "package_ndc": "60687-695-01", "marketing_end_date": "20260731", "marketing_start_date": "20230511"}], "brand_name": "Sucralfate", "product_id": "60687-695_37dbc9fb-25b5-30a2-e063-6294a90a78b8", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "60687-695", "generic_name": "Sucralfate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA074415", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20230511"}