Package 54766-895-03

Brand: lotronex

Generic: alosetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54766-895-03
Digits Only 5476689503
Product NDC 54766-895
Description

30 TABLET in 1 BOTTLE (54766-895-03)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand lotronex
Generic alosetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43143464-47b5-0b88-e063-6394a90a01ef", "openfda": {"upc": ["0354766894039", "0354766895036"], "unii": ["2F5R1A46YW"], "rxcui": ["259306", "261362", "403975", "540181"], "spl_set_id": ["35cbb9d5-639b-207a-e054-00144ff88e88"], "manufacturer_name": ["Sebela Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (54766-895-03)", "package_ndc": "54766-895-03", "marketing_end_date": "20260430", "marketing_start_date": "20160711"}], "brand_name": "LOTRONEX", "product_id": "54766-895_43143464-47b5-0b88-e063-6394a90a01ef", "dosage_form": "TABLET", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "54766-895", "generic_name": "alosetron hydrochloride", "labeler_name": "Sebela Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOTRONEX", "active_ingredients": [{"name": "ALOSETRON HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "NDA021107", "marketing_category": "NDA", "marketing_end_date": "20260430", "marketing_start_date": "20160711"}