Package 0254-3029-02

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 0254-3029-02
Digits Only 0254302902
Product NDC 0254-3029
Product ID 0254-3029_533199b4-1242-45a6-9cdd-5018052a399b
Description

60 CAPSULE, GELATIN COATED in 1 BOTTLE (0254-3029-02)

Marketing

Marketing Status
Marketed Since 2021-01-01
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": "533199b4-1242-45a6-9cdd-5018052a399b", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["9d958b58-6c4f-4bb1-8660-cf5eac256440"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (0254-3029-02)", "package_ndc": "0254-3029-02", "marketing_start_date": "20210101"}], "brand_name": "Lubiprostone", "product_id": "0254-3029_533199b4-1242-45a6-9cdd-5018052a399b", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "0254-3029", "generic_name": "Lubiprostone", "labeler_name": "Par Health USA, LLC", "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": "20210101", "listing_expiration_date": "20261231"}