Package 70518-3209-1
Brand: rabeprazole sodium
Generic: rabeprazole sodiumPackage Facts
Identity
Package NDC
70518-3209-1
Digits Only
7051832091
Product NDC
70518-3209
Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3209-1)
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": "3a253480-d339-fd62-e063-6394a90a7372", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["0e2e00fa-c4c5-4de7-adf9-cd9786b97016"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3209-0)", "package_ndc": "70518-3209-0", "marketing_start_date": "20210901"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3209-1)", "package_ndc": "70518-3209-1", "marketing_start_date": "20210921"}], "brand_name": "RABEPRAZOLE SODIUM", "product_id": "70518-3209_3a253480-d339-fd62-e063-6394a90a7372", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70518-3209", "generic_name": "rabeprazole sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RABEPRAZOLE SODIUM", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA204237", "marketing_category": "ANDA", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}