Package 50090-6887-0
Brand: rabeprazole sodium
Generic: rabeprazole sodiumPackage Facts
Identity
Package NDC
50090-6887-0
Digits Only
5009068870
Product NDC
50090-6887
Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6887-0)
Marketing
Marketing Status
Brand
rabeprazole sodium
Generic
rabeprazole sodium
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2fb92517-ad93-4385-aadc-33ce1b770a25", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["bafff1ac-02fb-4726-b2d7-6e099ae981cb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6887-0)", "package_ndc": "50090-6887-0", "marketing_start_date": "20231206"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6887-1)", "package_ndc": "50090-6887-1", "marketing_start_date": "20231206"}], "brand_name": "RABEPRAZOLE SODIUM", "product_id": "50090-6887_2fb92517-ad93-4385-aadc-33ce1b770a25", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-6887", "generic_name": "rabeprazole sodium", "labeler_name": "A-S Medication Solutions", "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": "20170601", "listing_expiration_date": "20261231"}