Package 70710-1642-1

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 70710-1642-1
Digits Only 7071016421
Product NDC 70710-1642
Description

100 CAPSULE in 1 BOTTLE (70710-1642-1)

Marketing

Marketing Status
Marketed Since 2023-03-23
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": "f06e99fa-9894-48ab-99d8-914987dbb73f", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["6c11a204-6831-4269-a3c4-1702ed83f74b"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70710-1642-1)", "package_ndc": "70710-1642-1", "marketing_start_date": "20230323"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (70710-1642-6)", "package_ndc": "70710-1642-6", "marketing_start_date": "20230323"}], "brand_name": "Lubiprostone", "product_id": "70710-1642_f06e99fa-9894-48ab-99d8-914987dbb73f", "dosage_form": "CAPSULE", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "70710-1642", "generic_name": "Lubiprostone", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "24 ug/1"}], "application_number": "ANDA214131", "marketing_category": "ANDA", "marketing_start_date": "20230323", "listing_expiration_date": "20261231"}