sucralfate

Generic: sucralfate

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-436
Product ID 62135-436_3ba3bac9-79bb-7f76-e063-6294a90a4d32
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)
aluminum complex [epc]
Chemical Structure
organometallic compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135436
Hyphenated Format 62135-436

Supplemental Identifiers

RxCUI
314234
UPC
0362135436902 0362135436018
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 ANDA074415 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (62135-436-01)
  • 90 TABLET in 1 BOTTLE (62135-436-90)
source: ndc

Packages (2)

62135-436-01 100 TABLET in 1 BOTTLE (62135-436-01) 62135-436-90 90 TABLET in 1 BOTTLE (62135-436-90)

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": "3ba3bac9-79bb-7f76-e063-6294a90a4d32", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0362135436902", "0362135436018"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["30c0965a-02a0-46b5-aa09-3f5fb5047b22"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62135-436-01)", "package_ndc": "62135-436-01", "marketing_start_date": "20230313"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-436-90)", "package_ndc": "62135-436-90", "marketing_start_date": "20221104"}], "brand_name": "Sucralfate", "product_id": "62135-436_3ba3bac9-79bb-7f76-e063-6294a90a4d32", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "62135-436", "generic_name": "Sucralfate", "labeler_name": "Chartwell RX, LLC", "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"}