Package 63304-352-60

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 63304-352-60
Digits Only 6330435260
Product NDC 63304-352
Product ID 63304-352_4097ef5c-5f08-e436-e063-6294a90a692a
Description

60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-352-60)

Marketing

Marketing Status
Marketed Since 2023-01-01
Brand lubiprostone
Generic lubiprostone
Sample Package No

Linked Drug Pages (1)

Lubiprostone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4097ef5c-5f08-e436-e063-6294a90a692a", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["f06d76d2-028a-629f-e053-2995a90a80f5"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-352-60)", "package_ndc": "63304-352-60", "marketing_start_date": "20230101"}], "brand_name": "Lubiprostone", "product_id": "63304-352_4097ef5c-5f08-e436-e063-6294a90a692a", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "63304-352", "generic_name": "lubiprostone", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "24 ug/1"}], "application_number": "NDA021908", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20230101", "listing_expiration_date": "20261231"}