sucralfate

Generic: sucralfate

Labeler: mylan pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler mylan pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Mylan Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 59762-0401
Product ID 59762-0401_311db6f8-1bc9-46af-a866-d7ad4d8193dc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018333
Listing Expiration 2027-12-31
Marketing Start 2017-09-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 597620401
Hyphenated Format 59762-0401

Supplemental Identifiers

RxCUI
314234
UPC
0359762040114 0041200002760
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 (source: ndc)
Application Number NDA018333 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59762-0401-1)
  • 500 TABLET in 1 BOTTLE (59762-0401-5)
source: ndc

Packages (2)

59762-0401-1 100 TABLET in 1 BOTTLE (59762-0401-1) 59762-0401-5 500 TABLET in 1 BOTTLE (59762-0401-5)

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": "311db6f8-1bc9-46af-a866-d7ad4d8193dc", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0359762040114", "0041200002760"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["ae58c382-c1cf-4ebf-9c97-bdff0682df8b"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59762-0401-1)", "package_ndc": "59762-0401-1", "marketing_start_date": "20170925"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59762-0401-5)", "package_ndc": "59762-0401-5", "marketing_start_date": "20170925"}], "brand_name": "Sucralfate", "product_id": "59762-0401_311db6f8-1bc9-46af-a866-d7ad4d8193dc", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "59762-0401", "generic_name": "Sucralfate", "labeler_name": "Mylan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "NDA018333", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20170925", "listing_expiration_date": "20271231"}