sucralfate

Generic: sucralfate

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1833
Product ID 70771-1833_f0b6479d-234b-426c-8035-6e4675d8853a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215705
Listing Expiration 2026-12-31
Marketing Start 2023-05-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711833
Hyphenated Format 70771-1833

Supplemental Identifiers

RxCUI
314234
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 ANDA215705 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70771-1833-1)
  • 30 TABLET in 1 BOTTLE (70771-1833-3)
  • 500 TABLET in 1 BOTTLE (70771-1833-5)
source: ndc

Packages (3)

70771-1833-1 100 TABLET in 1 BOTTLE (70771-1833-1) 70771-1833-3 30 TABLET in 1 BOTTLE (70771-1833-3) 70771-1833-5 500 TABLET in 1 BOTTLE (70771-1833-5)

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": "f0b6479d-234b-426c-8035-6e4675d8853a", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["882b7596-f62c-4be2-8f67-e64310718baa"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1833-1)", "package_ndc": "70771-1833-1", "marketing_start_date": "20230520"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1833-3)", "package_ndc": "70771-1833-3", "marketing_start_date": "20230520"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1833-5)", "package_ndc": "70771-1833-5", "marketing_start_date": "20230520"}], "brand_name": "Sucralfate", "product_id": "70771-1833_f0b6479d-234b-426c-8035-6e4675d8853a", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "70771-1833", "generic_name": "Sucralfate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA215705", "marketing_category": "ANDA", "marketing_start_date": "20230520", "listing_expiration_date": "20261231"}