Package 68462-827-61

Brand: sucralfate oral suspension

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 68462-827-61
Digits Only 6846282761
Product NDC 68462-827
Product ID 68462-827_1e595c2a-edd0-43f7-a2db-69553b9557d9
Description

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

Marketing

Marketing Status
Marketed Since 2026-01-05
Brand sucralfate oral suspension
Generic sucralfate
Sample Package No

Linked Drug Pages (1)

Sucralfate oral suspension ndc-match (0.95)

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"}