Package 68788-7459-6
Brand: rabeprazole sodium
Generic: rabeprazole sodiumPackage Facts
Identity
Package NDC
68788-7459-6
Digits Only
6878874596
Product NDC
68788-7459
Description
60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7459-6)
Marketing
Marketing Status
Brand
rabeprazole sodium
Generic
rabeprazole sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "20aadee0-d25c-4e62-b543-62b344a2fbdf", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["ac9266ed-a9b2-4e77-8607-393b5dcdd2b6"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7459-3)", "package_ndc": "68788-7459-3", "marketing_start_date": "20191227"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7459-6)", "package_ndc": "68788-7459-6", "marketing_start_date": "20191227"}], "brand_name": "Rabeprazole Sodium", "product_id": "68788-7459_20aadee0-d25c-4e62-b543-62b344a2fbdf", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68788-7459", "generic_name": "Rabeprazole Sodium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole Sodium", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA208644", "marketing_category": "ANDA", "marketing_start_date": "20180427", "listing_expiration_date": "20261231"}