sucralfate

Generic: sucralfate

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sucralfate 1 g/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-2210
Product ID 0093-2210_c363786b-0fde-45c0-9575-2a4ca71aa592
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070848
Listing Expiration 2026-12-31
Marketing Start 1996-11-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00932210
Hyphenated Format 0093-2210

Supplemental Identifiers

RxCUI
314234
UPC
0300932210981
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 ANDA070848 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-2210-01)
  • 500 TABLET in 1 BOTTLE (0093-2210-05)
  • 90 TABLET in 1 BOTTLE (0093-2210-98)
source: ndc

Packages (3)

0093-2210-01 100 TABLET in 1 BOTTLE (0093-2210-01) 0093-2210-05 500 TABLET in 1 BOTTLE (0093-2210-05) 0093-2210-98 90 TABLET in 1 BOTTLE (0093-2210-98)

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": "c363786b-0fde-45c0-9575-2a4ca71aa592", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0300932210981"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["c7a43df7-eb37-4273-9250-87953b1fd270"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-2210-01)", "package_ndc": "0093-2210-01", "marketing_start_date": "19961111"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0093-2210-05)", "package_ndc": "0093-2210-05", "marketing_start_date": "19961111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0093-2210-98)", "package_ndc": "0093-2210-98", "marketing_start_date": "20110112"}], "brand_name": "Sucralfate", "product_id": "0093-2210_c363786b-0fde-45c0-9575-2a4ca71aa592", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "0093-2210", "generic_name": "Sucralfate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA070848", "marketing_category": "ANDA", "marketing_start_date": "19961111", "listing_expiration_date": "20261231"}