sucralfate

Generic: sucralfate

Labeler: torrent pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler torrent pharmaceuticals limited
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-754
Product ID 13668-754_fd033c55-d1ae-4fbb-82ad-b092a20bb7e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216726
Listing Expiration 2026-12-31
Marketing Start 2025-09-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13668754
Hyphenated Format 13668-754

Supplemental Identifiers

RxCUI
313123
UPC
0313668754421
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 ANDA216726 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 420 mL in 1 BOTTLE (13668-754-42)
source: ndc

Packages (1)

Ingredients (1)

sucralfate (1 g/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fd033c55-d1ae-4fbb-82ad-b092a20bb7e8", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0313668754421"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["dc361b46-fda4-4b0b-9950-e8885ba5b084"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (13668-754-42)", "package_ndc": "13668-754-42", "marketing_start_date": "20250915"}], "brand_name": "Sucralfate", "product_id": "13668-754_fd033c55-d1ae-4fbb-82ad-b092a20bb7e8", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "13668-754", "generic_name": "Sucralfate", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA216726", "marketing_category": "ANDA", "marketing_start_date": "20250915", "listing_expiration_date": "20261231"}