Package 72189-142-90
Brand: rabeprazole sodium
Generic: rabeprazole sodiumPackage Facts
Identity
Package NDC
72189-142-90
Digits Only
7218914290
Product NDC
72189-142
Description
90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-142-90)
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": "2be9206c-ed86-e301-e063-6294a90a43a8", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["b1b7def0-834f-37f5-e053-2a95a90ade1f"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-142-30)", "package_ndc": "72189-142-30", "marketing_start_date": "20201015"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-142-90)", "package_ndc": "72189-142-90", "marketing_start_date": "20201015"}], "brand_name": "RABEPRAZOLE SODIUM", "product_id": "72189-142_2be9206c-ed86-e301-e063-6294a90a43a8", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-142", "generic_name": "RABEPRAZOLE SODIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RABEPRAZOLE SODIUM", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA205761", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}