Package 43598-163-60

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 43598-163-60
Digits Only 4359816360
Product NDC 43598-163
Description

60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-163-60)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "006d4453-ecae-42d5-8242-9508daaef937", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["006b8b6c-f0eb-4246-87da-67582984b0e4"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-163-60)", "package_ndc": "43598-163-60", "marketing_start_date": "20230101"}], "brand_name": "Lubiprostone", "product_id": "43598-163_006d4453-ecae-42d5-8242-9508daaef937", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "43598-163", "generic_name": "Lubiprostone", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "8 ug/1"}], "application_number": "NDA021908", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20230101", "listing_expiration_date": "20261231"}