Package 68788-7742-8

Brand: lansoprazole

Generic: lansoprazole
NDC Package

Package Facts

Identity

Package NDC 68788-7742-8
Digits Only 6878877428
Product NDC 68788-7742
Description

120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-8)

Marketing

Marketing Status
Marketed Since 2020-07-01
Brand lansoprazole
Generic lansoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef4a11a3-db2c-4c0b-b08c-8efb4493d5a6", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277"], "spl_set_id": ["7286d6a5-611b-4993-ab93-4899d599435d"], "pharm_class_pe": ["Inhibition Gastric Acid Secretion [PE]"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-1)", "package_ndc": "68788-7742-1", "marketing_start_date": "20200701"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-3)", "package_ndc": "68788-7742-3", "marketing_start_date": "20200701"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-6)", "package_ndc": "68788-7742-6", "marketing_start_date": "20200701"}, {"sample": false, "description": "120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-8)", "package_ndc": "68788-7742-8", "marketing_start_date": "20200701"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-9)", "package_ndc": "68788-7742-9", "marketing_start_date": "20200701"}], "brand_name": "Lansoprazole", "product_id": "68788-7742_ef4a11a3-db2c-4c0b-b08c-8efb4493d5a6", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68788-7742", "generic_name": "Lansoprazole", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lansoprazole", "active_ingredients": [{"name": "LANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA205868", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}