Package 72865-257-30

Brand: fingolimod

Generic: fingolimod
NDC Package

Package Facts

Identity

Package NDC 72865-257-30
Digits Only 7286525730
Product NDC 72865-257
Description

30 CAPSULE in 1 BOTTLE (72865-257-30)

Marketing

Marketing Status
Marketed Since 2024-06-17
Brand fingolimod
Generic fingolimod
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b506d53-7362-2b6a-e063-6394a90a0a69", "openfda": {"upc": ["0372865257302"], "unii": ["G926EC510T"], "rxcui": ["1012895"], "spl_set_id": ["c5402dd1-c496-405d-9cae-07ccf184339c"], "manufacturer_name": ["XLCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72865-257-30)", "package_ndc": "72865-257-30", "marketing_start_date": "20240617"}], "brand_name": "Fingolimod", "product_id": "72865-257_1b506d53-7362-2b6a-e063-6394a90a0a69", "dosage_form": "CAPSULE", "pharm_class": ["Sphingosine 1-Phosphate Receptor Modulators [MoA]", "Sphingosine 1-phosphate Receptor Modulator [EPC]"], "product_ndc": "72865-257", "generic_name": "Fingolimod", "labeler_name": "XLCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fingolimod", "active_ingredients": [{"name": "FINGOLIMOD HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA207933", "marketing_category": "ANDA", "marketing_start_date": "20240617", "listing_expiration_date": "20261231"}