Package 50090-4751-0
Brand: rabeprazole sodium
Generic: rabeprazole sodiumPackage Facts
Identity
Package NDC
50090-4751-0
Digits Only
5009047510
Product NDC
50090-4751
Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-0)
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": "e50376c6-3db4-429f-bf11-982f49d5e4df", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["4ded337a-31b8-47c3-b5ab-33a785afb7d8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-0)", "package_ndc": "50090-4751-0", "marketing_start_date": "20191125"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-1)", "package_ndc": "50090-4751-1", "marketing_start_date": "20191125"}], "brand_name": "Rabeprazole Sodium", "product_id": "50090-4751_e50376c6-3db4-429f-bf11-982f49d5e4df", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-4751", "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": "ANDA208644", "marketing_category": "ANDA", "marketing_start_date": "20180427", "listing_expiration_date": "20261231"}