sucralfate oral suspension

Generic: sucralfate

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

Drug Facts

Product Profile

Brand Name sucralfate oral suspension
Generic Name sucralfate
Labeler glenmark pharmaceuticals inc., usa
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Glenmark Pharmaceuticals Inc., USA

Identifiers & Regulatory

Product NDC 68462-827
Product ID 68462-827_1e595c2a-edd0-43f7-a2db-69553b9557d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212141
Listing Expiration 2027-12-31
Marketing Start 2026-01-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68462827
Hyphenated Format 68462-827

Supplemental Identifiers

RxCUI
313123
UPC
0368462827611
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 oral suspension (source: ndc)
Generic Name sucralfate (source: ndc)
Application Number ANDA212141 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 420 mL in 1 BOTTLE (68462-827-61)
source: ndc

Packages (1)

68462-827-61 420 mL in 1 BOTTLE (68462-827-61)

Ingredients (1)

sucralfate (1 g/10mL)

Linked Drug Pages (1)

Sucralfate oral suspension ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1e595c2a-edd0-43f7-a2db-69553b9557d9", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0368462827611"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["1e595c2a-edd0-43f7-a2db-69553b9557d9"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (68462-827-61)", "package_ndc": "68462-827-61", "marketing_start_date": "20260105"}], "brand_name": "Sucralfate oral suspension", "product_id": "68462-827_1e595c2a-edd0-43f7-a2db-69553b9557d9", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68462-827", "generic_name": "sucralfate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate oral suspension", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA212141", "marketing_category": "ANDA", "marketing_start_date": "20260105", "listing_expiration_date": "20271231"}